All papers that have been chosen for oral presentation, the top ten candidates for the best poster award and the 42 best posters will be published in an open-access online edition of Hormone Research in Pediatrics, one of the leading scientific journals in the field of Pediatric Endocrinology

Oral Presentation

OP1 - Clinical presentation and genetic findings in the Paraganglioma Syndrome associated with mutations in SDHB (Pgl4)
Autor(es): Sanso G; Vieites A; De Miguel V; Bergada I; Barontini M;

OP2 - Predictive Cut Off Values of Basal 17-hydroxyprogesterone (17OHP) to Diagnose Non-Classic Congenital Adrenal Hyperplasia due to 21-Hydroxilase Deficiency
Autor(es): Chagas NB; Braid ZM; Coeli-Lacchini F; Castro M; Moreira AC; Mermejo LM; Antonini SR;

OP3 - SAMD9 (Sterile Alpha Motif Domain-containing 9) in Adrenocortical Tumors
Autor(es): Santos CH; Bueno AC; More CB; Stecchini MF; Ramalho LZ; Ramalho F; Moreira AC; Castro M; Brandalise S; Yunes A; Antonini SR;

OP4 - VALIDATION OF SERUM 17α-HYDROXYPROGESTERONE CONCENTRATION REFERENCE RANGES BY ELISA METHOD IN INFANTS DURING THE FIRST YEAR OF LIFE
Autor(es): Cestino ML; Breyer FA;

OP5 - INHIBITION OF IGF1R BY IGF-1R/IR INHIBITOR OSI906 AS A TARGETED THERAPY FOR GLIOBLASTOMA: IN VITRO & IN VIVO STUDIES.
Autor(es): Fernández MC; Martin A; Clément F; Venara MC; García Lombardi M; Bergadá I; Gutiérrez M; Pennisi PA;

OP6 - Bone age determination in Brazilian children and adolescents: a comparison between computerized BoneXpert, Greulich-Pyle and Tanner-Whitehouse II methods.
Autor(es): Artioli TO; Morais TK; Kochi C; Longui CA;

OP7 - Chromosomal IGF1R deletion: array characterization in two patients with structural abnormalities in chromosome 15
Autor(es): Casali B; Keselman A; Villegas F; Sanguineti, Nora; Fernandez MC; Armando R; Boywitt A; Rodolfo De Bellis; del Rey G; Arberas C; Rey R; Ropelato G; Bergadá, I;

OP8 - Clinical and genetic evaluation of prepubertal children with short stature and advanced bone age
Autor(es): Vasques GA; Andrade NLM; Funari MFA; Homma TK; Freire BL; Nishi MY; Malaquias AC; Mendonca BB; Arnhold IJP; Jorge AAL;

OP9 - Clinical aspects and common genetics polymorphisms implicated in short stature in sickle cell anemia
Autor(es): Costa-Júnior DA; Frossard TNSV; Rodrigues TMB; Santos APP; Amaral AB; Silva CM; Ferreira FO; Carvalho GQ; Madeira M; Velloso-Rodrigues C; Silva IT; Lima RLS; Cruz NRC; Neto LH;

OP10 - CONGENITAL AND ACQUIRED PITUITARY INSUFFICIENCY DURING THE TRANSITION STAGE: FIRST ARGENTINE EXPERIENCE IN THE EVALUATION OF CARDIOMETABOLIC PARAMETERS AT THE END OF GH THERAPY
Autor(es): Boquete C; Boquete HR; Sequera AM; Ruibal G; Suárez M; Azaretzky M; Fideleff G; Dzembrowski L; Nuñez Chavarria E; Fideleff HL;

OP11 - Evidence-based approach for current standardized GH, IGF-I and IGFBP-3 assays to rule out GHD in neonates and infants.
Autor(es): Braslavsky D; Keselman A; Rodriguez ME; Freire AV; Altube M; Gutierrez A; Scaglia PA; Gotta G; Ropelato MG; Bergadá I; Ballerini MG;

OP12 - Heterozygous GH1 p.R209H variant challenges the assessment of short stature
Autor(es): Braslavsky D; Sanguineti N; Scaglia P; Keselman A; Ballerini MG; Ropelato MG; Suco S; Kitzman J; Vishnopolska S; Marti M; Domené H; Rey R; Perez Millan MI; Camper SA;

OP13 - Novel familial ACAN gene mutation in a short stature family of an SGA proband
Autor(es): Kraus J; Dauber A; Hwa V; Tyzinski L; Fujimoto M;

OP14 - RESPONSE TO rhGH THERAPY IN CHILDREN WITH ISOLATED SHORT STATURE WITH OR WITHOUT AN IDENTIFIED GENETIC CAUSE
Autor(es): Andrade NLM; Vasques GA; Funari MFA; Menconca BB; Jorge AAL;

OP15 - The overweight and obesity accelerates de skeletal maturity and decrease the growth potential in Mexican children and adolescents.
Autor(es): Miranda-Lora AL; Espinosa- Espindola M; López- González D; Sánchez Curiel- Loyo Mariana; Dies-Suárez P ; Klünder- Klünder M;

OP16 - 24-hour glucose profile in healthy adults using a continuous glucose monitoring system.
Autor(es): Gaete X; CERDA T; ROMAN R.; CODNER E.;

OP17 - Acquired lipodystrophy among children and adolescents attending a diabetes camp
Autor(es): Werneck G; Dos Santos TJ; Salazar-González JJ; Pumputis FRC; Palacio J; Coll J; López M;

OP18 - BMI TRAJECTORY FROM BIRTH TO ADULTHOOD AND ITS ASSOCIATION WITH PANCREATIC β-CELL FUNCTION IN EARLY ADULTHOOD
Autor(es): BURROWS R; CORREA-BURROWS R; ROGAN J; BLANCO E; GAHAGAN S;

OP19 - CONGENITAL HYPERINSULINEMIC HYPOGLUCEMIA, OUR EXPERIENCE IN 34 PATIENTS
Autor(es): Barreto TG; Calzada R; Ruiz M; Arguinzoniz L; Altamirano N; Medina FA; Flanagan S; Aguilar L; Nishimura E;

OP20 - Development and validation of an educative manual for adolescents with type 2 diabetes.
Autor(es): Hernández Trejo KE ; Medina Bravo PG; Ibarra Delgado A; Velázquez López L; Lam Chávez AE;

OP21 - FOLLOW-UP OF PATIENTS WITH TYPE 1 DIABETES MELLITUS WHO UNDERWENT INSULIN PUMP TRAINING IN A PEDIATRIC ENDOCRINOLOGY CENTER
Autor(es): Cespedes C; Pavia MA; Forero C ; Coll M; Duran P;

OP22 - Insulin glargine 300 U/mL (Gla-300) provides effective glycemic control in youths with type 1 diabetes (T1D): the EDITION JUNIOR study
Autor(es): Danne, T; Tamborlane WT; Malievsky O; Franco D; Kawamura T; Demissie M; Niemoeller E; Goyeau H; Wardecki M; Battelino T;

OP23 - Longitudinal assessment of Klotho, FGF21, Adiponectin (Adp) and C-reactive-protein (CRP) levels in adolescents and young women with type 1 diabetes (T1D) using contraception.
Autor(es): Iñiguez G; Giraudo F; Salinas A; Merino P; Castro A; López P; Lardone MC; Cassorla F; Codner E;

OP24 - Variability in basal insulin needs in young patients with type 1 diabetes using continuous subcutaneous insulin infusion and continuous glucose monitoring with predictive low glucose insulin suspension
Autor(es): De Tezanos-Pinto A; Pichott M; Barra A; Avila A; Cassorla F; Codner E; Gaete X; Mericq V; Roman R;

OP25 - An extremely rare novel missense variant p.M304V in SOX3 gene is responsible for an X-linked GH deficiency in a Brazilian patient
Autor(es): Benedetti AFF; Silva JM; Biscotto IP; Ferreira NP; Arnhold IJP; Mendonca BB; Carvalho LRS;

OP26 - Probably Pathogenic Variants in New Candidate Genes in Patients with Pituitary Stalk Interruption Syndrome (PSIS) revealed by Whole-Exome Sequencing
Autor(es): Correa FA; Nakaguma M; Jorge AAL; Funari MFA; Lerario AM; Carvalho LRS; Arnhold IJP; Mendonca BB;

OP27 - Use of Desmopressin for Bilateral Inferior Petrosal Sinus Sampling (BIPSS) in Pediatric Patients with Cushing Disease (CD).
Autor(es): Di Palma MI; Plomer P; Gil S; Vaiani E; Viterbo G; Requejo F; Gonzalez Ramos J; Lazzati JM; Lubieniecki F; Rugilo C; Ciaccio M;

OP28 - Etiologies and clinical presentation of persistent hypoparathyroidism (HPT) in 61 children in a single tertiary center
Autor(es): Soto MF; Aziz M; Herzovich V; Dujovne N; Gazek N; Gutièrrez G; Ramirez P; Oleastro M; Obregon MG; Ayarzabal V; Ciaccio M; Gil S; Viterbo G;

OP29 - Hypercalcemia secondary to disseminated BCGitis in a boy with Mendelian Susceptibility to Mycobacteria (MSMD) due to mutation in IFN-ɣ receptor 1 gene (IFNGR1)
Autor(es): Soto MF; Mattone MC; Morales CA; Oleastro M; Palma A; Urdinez L; Viterbo GL;

OP30 - Neonatal multiple bone fractures and respiratory distress secondary to congenital hyperparathyroidism
Autor(es): Plomer PG; Soto MF; De Dona V; Dujovne N; Gil S; Vaiani E; Viterbo G;

OP31 - Osteogenesis imperfecta type I: which patients should be treated with aminobisphosphonates?
Autor(es): Santos IN; Menezes Filho HC ; Franco, RR; Cominato L; Steinmetz L; Manna TD; Damiani D;

OP32 - Use of anti-FGF23 monoclonal antibody in the treatment of children and adolescents with X-Linked Hypophosphatemic Rickets.
Autor(es): Hamilton; L Brenzoni; V Forclaz; S D´Amato; Rosenfeld P; Bergada I; Alconcher L;

OP33 - BMI throughout the life-course and its relation with cardiometabolic disorders in early adulthood: results from the Santiago Longitudinal Study
Autor(es): BURROWS R; CORREA-BURROWS P; ROGAN J; BLANCO E; GAHAGAN S;

OP34 - Changes on Gut Microbiota After Laparoscopic Sleeve Gastrectomy in Adolescence: Case Reports.
Autor(es): Rachid L; Cominato L; Franco RR; Cortez RV; Moreira LN; Frascino A; Taddei CR; Steinmetz L; Della Manna T; Velhote MCP; Filho HCM; Toma RK; Damiani D;

OP35 - Differences between short- and long-term outcomes of laparoscopic sleeve gastrectomy in adolescence.
Autor(es): Franco RR; Cominato L; Ybarra M; Rachid L; Jeronimo T; Potter M; Steinmetz L; Manna TD; Menezes Filho HC; velhote MC; Durval D;

OP36 - Nonalcoholic Fatty Liver Disease and morbid obese adolescent submitted to a bariatric surgery.
Autor(es): Cominato L; Franco RR; rachid l; Frascino A; Leandra Steinmetz; Manna TD; Velhote MC; Menezes Filho HC; ybarra m; Deboni M; Toma RK; Porta G; Damiani D;

OP37 - 47,XXY/46,XX chromosomal DSD: challenges in the diagnosis and management
Autor(es): Bastida MG; Grinspon R; Avila S; De Carli C; Diaz S; Venara M; Bergada I; Rey MR;

OP38 - A Novel Anti-Müllerian Hormone (AMH) Gene Mutation in a Patient with Persistent Müllerian Duct Syndrome (PMDS) type 1
Autor(es): Mattone MC; Lobo de la Vega V; D’Alessandro P; Marino R; Perez Garrido N; Galluzzo ML; Costanzo M; Zaidman V; Lazzati JM; Berensztein E; Ramirez P; Touzon MS; Ciaccio M; Belgorosky A; Bailez M; Guercio G;

OP39 - Characteristics of transgender children and adolescent patients in a pediatric hospital: Multidisciplinary approach
Autor(es): Figueroa Gacitúa V; Sanz C; Nigro N; Lopez Dacal J; Gallardo R; Brunetto O H;

OP40 - DHX37: a new player in 46,XY gonadal dysgenesis
Autor(es): Costanzo M; Guercio G; Touzon MS; Marino R; Mattone C; Ramirez P; Perez Garrido N; Lazzati JM; Zaidman V; Galluzo L; Bailez M; Berensztein E; Ciaccio M; Belgorosky A;

OP41 - DSD, BONE DYSPLASIA, AND THE Y CHROMOSOME?
Autor(es): Mendoza Rojas VC; Contreras García GA;

OP42 - Evaluation of puberty in patients with Noonan syndrome and mutations in the RAS/MAPK genes.
Autor(es): Malaquias AC; Noronha RM; Homma TK; Albuquerque EVA; Vasques GA; Bertola DR; Jorge AAL;

OP43 - Puberty and Growth in Boys with Constitutional Delay of Growth and Puberty
Autor(es): Luciano TM; Stecchini MF; de Almeida LEA; Bettiol H; Cardoso VC; Aragon DC; Antonini SR;

OP44 - Safety of chemotherapy for hematologic malignancies as regards testicular endocrine function in children and teenagers
Autor(es): Romina P. Grinspon; María Arozarena; Silvina Prada; Graciela Bargman; María Sanzone; Marjorie Morales Bazurto; Marcela Gutiérrez; Patricia Bedecarrás; Ana Kannemann; Graciela O. Elena ; Silvia Gottlieb; Ariel J. Berenstein; María Gabriela Ropelato; Ignacio Bergadá; Luis A. Aversa; Rodolfo A. Rey;

OP45 - EVALUATION OF PUBLIC CONGENITAL HYPOTHYROIDISM SCREENING PROGRAM IN SOUTHERN BRAZIL AFTER TSH CUTOFF REDUCTION
Autor(es): Rizzotto MIB; Carreiro S; Garcia RMR; Selistre L; Vargas PR; Mastella L; Castro SM; Kopacek C;

OP46 - Factors associated with neonatal hyperthyroidism in neonates born to mothers with Graves‘ disease
Autor(es): Munoz T; Roman R;

OP47 - Male individuals with Autoimmune Thyroid Disease present higher risk for clustering other Non-Thyroidal Autoimmune Diseases
Autor(es): Lopes FSC; Almeida MAAL; Pratesi R; Oliveira RS; Castro LC;

OP48 - The usefulness of free T3 and free T3/free T4 ratio in the differential diagnosis between non-thyroidal illness and central hypothyroidism in pediatric children
Autor(es): Garín Gómez S; Zaidman V; Herzovich V; Dujovne N; Gazek N; Florio S; Belgorosky A; Ciaccio M; Lazzati JM;



Poster presentation

Adrenal

PP1 - Childhood adrenocortical carcinoma: Case report
Autor(es): Ana Rocha R.; Carolina Sepulveda R.; Andrea Perez; Vivian Gallardo; Soledad VillanuevaT.; Anahi Yizmeyian;

PP2 - Clinical and biochemical features at the diagnosis of a large cohort of patients diagnosed with the classic form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Autor(es): Braid, Zilda; CASTRO, M; MERMEJO, LÍVIA M.; ANTONINI, S R.; MOREIRA, A. C;

PP3 - Congenital Adrenal Hyperplasia (CAH): Case report of a compound heterozygote CYP21A2 mutation with high glucocorticoids (GC) sensibility
Autor(es): Obeid BL; Castro ABS; Franco RR; Cominato L; Steinmetz L; Manna TD; Filho HCM; Semer B; Carvalho DF; Bachega T; Damiani D;

PP4 - CONGENITAL ADRENAL HYPERPLASIA: Clinical and molecular profile of newborns detected after 5 years of public screening program implementation
Autor(es): Kopacek C; Beltrão LA; Wiest P; Vargas PR; Krebs I; Castro SM;

PP5 - Differential Diagnosis of Virilization in Prepubertal Children: Case Report
Autor(es): Bordin L; Bitencourt BB; Ferreira R; Oliveira LS; França FV; Hasselmann PF; Kraemer GC; França SN; Pereira RM;

PP6 - Early diagnosis of adrenocortical carcinoma due to elevated 17-hydroxyprogesterone in newborn screening.
Autor(es): Garcia TS; Erbes JM; Lee JS; Cechinel E; Simoni G; Nascimento ML ; Silva PCA;

PP7 - Experience in a Screening program for Congenital Adrenal Hyperplasia between 2010-2018
Autor(es): Vitale LE; Gonzalez V; Morín A; Tournier A; Borrajo G; Marino R; Belgorosky A; Santucci Z; Balbi V; Fasano MV;

PP8 - IN2 AND V281L MUTATION OF THE CYP21A2 GEN AS A CAUSE OF SUPRARENAL HYPERPLASIA
Autor(es): Mejia de Beldjenna L; Contreras D; Perez MC ; Rios C;

PP9 - Initial assessment of patients with high levels of 17-alpha-hydroxyprogesterone (17-OHP) at neonatal screening (NS): Clinical and laboratorial profile
Autor(es): Diniz ALO; Costa MW; Cabral Menezes-Filho H; Franco, RR; Steinmetz L; Cominato L; Della Manna T; Damiani D;

PP10 - Prevalence of polymorphisms of the NR3C1 gene related to glucocorticoid sensitivity in patients with congenital adrenal hyperplasia
Autor(es): Soares NF; Villela TR; Barra CB; Silva ACS; Belisário AR; Silva IN;

PP11 - Revisiting incidence of congenital adrenal hyperplasia in the State of Minas Gerais - Brazil
Autor(es): Soares NF; Ferreira TL; Mafra JR; Oliveira LE; Silva LCB; Barra CB; Mantovani RM; Pezzuti IL; Silva IN;

PP12 - Slow progression of a large adrenocortical carcinoma in a pediatric patient
Autor(es): Lopez Dacal J; Gallardo R; Cassanova A; Basile C; Denes E; Navacchia D; Brunetto O; Figueroa Gacitua V;

PP13 - UNCOMMON FINDINGS IN BECKWITH-WIEDEMANN SYNDROME
Autor(es): ERBES JM; GARCIA TS; LEE JS; CECHINEL E; SIMONI G; NASCIMENTO ML; SILVA PCA;

PP14 - VIRILIZATION IN AN ADOLESCENT GIRL: OVARIAN HYPERTHECOSIS?
Autor(es): Oliveira LS; França FV; Hasselmann PF; Bordin L; Kraemer GC; Carvalho JAR; Pereira RM; Franla SN; Demartini AC; Lacerda Filho L;


Growth

PP15 - A girl with short stature
Autor(es): Morales, CA; Costanzo M; Ciaccio M; Di Palma MI;

PP16 - Adherence and long-term outcomes of therapy in pediatric subjects in Argentina using easypod™ electromechanical device for growth hormone treatment: the Phase IV multicentre Easypod™ Connect Observational Study (ECOS)
Autor(es): C.Chareca; A.Belgorosky; J.Chiarpenello; L.Colombi; T. Pasqualini; C.Von Schulz Hausmann; A.Assefi; M.Miras;

PP17 - ANALYSIS OF SURVEY CARRIED OUT TO CHILEAN PROFESSIONALS ON THE PERCEPTION OF ADHERENCE OF PEDIATRIC PATIENTS TREATED WITH GROWTH HORMONE
Autor(es): De Tezanos-Pinto A; Hernandez MI;

PP19 - Excellent response to Growth Hormone and GnRH analogue treatment in a patient with Floating Harbor Syndrome
Autor(es): Aziz M; Plomer PG; Obregon MG; Ciaccio M;

PP20 - Growth and clinical characteristics of children with Floating-Harbor syndrome: analysis of current original data and a review of the literature
Autor(es): Malaquias AC; Homma TK; Freire BL; Honjo R; Dauber A; Funari MFA; Lerario AM; Albuquerque EV; Vasques GA; Bertola DR; Kim CA; Jorge AAL;

PP21 - Growth hormone (GH) therapy in disproportionate short children with skeletal dysplasias
Autor(es): Arruda BF; Malaquias, AC; Cabral, MM; Padua, JR; Gurjao, MM;

PP22 - Growth hormone treatment adherence in patients from an emerging economy country: 1-year real-world data from the easypod™ connect eHealth platform
Autor(es): Calliari, LEP; Barquero, P; Sato, C;

PP23 - Growth response and pubertal development in children with Growth Hormone deficiency and spontaneous puberty
Autor(es): Reinoso AS; Ricci J; Martín R; Fasano MV; Morín A; Balbi VA;

PP24 - Positive impact on adherence through educational activities of the Argentina´s Patient Support Program in children with low adherence to treatment with recombinant Growth Hormone (easypod applicator).
Autor(es): A.Assefi; C.Chareca; F.Roca; P.Celis Ayala; A.Rubstein; C.Von Schulz Hausmann;

PP25 - PROFILE OF PATIENTS TREATED WITH RECOMBINANT GROWTH HORMONE IN A REFERRAL CENTER
Autor(es): Batschauer A; Baroncini CV; Lacerda Filho L; França SN; Pereira RM; Demartini AC; Kraemer GC; Cat MNL; Carvalho JAR;

PP26 - Treatment With Growth Hormone in Mexican Girls With Turner Syndrome.
Autor(es): POSADAS MENDOZA KJ; Bonilla Medina PS ; Ruiz Reyes ML ; Calzada-León R; Arguinzoniz-Valenzuela SL ; Robles Valdés C;

PP27 - Validation of the parenteral presentation of clonidine for oral use in growth hormone provocative test
Autor(es): Fittipaldi Y.; Troiano M.; Kuspiel MF; Pasqualini T.; Alonso G.;


Diabetes and hypoglycemia

PP28 - Acute Disseminated Encephalomyelitis (ADEM) preceding Type 1 Diabetes: What is the role of anti-GAD?
Autor(es): Rossi ICB; Fernandes RGAL; Carvalho LC; Gomes DC;

PP29 - Association between hyperinsulinemia and Helicobacter pylori infection
Autor(es): Hayes Dorado JP; Rossell Lopez MA; Vaca Torruella M; Frias Eid OD; Urizar Parada V;

PP30 - Association between IGF-1 and non-alcoholic fatty liver disease in adolescents with type 2 diabetes mellitus
Autor(es): Martínez LG; Orozco JA; Medina PG;

PP31 - Changing the management of neonatal diabetes by means of genetic studies
Autor(es): Mejia L; Acevedo G; Astudillo E; Corredor V;

PP32 - Chronic mucocutaneous candidiasis and type 1 Diabetes in a child with STAT1 gain of function heterozygous mutation.
Autor(es): Pires JVG; Rodrigues R; Segundo GR; Gomes DC;

PP33 - Clinical and laboratory characteristics in Mexican adolescents with newly diagnosed Type 2 Diabetes.
Autor(es): Barrientos-Perez M; Gonzalez-Moreno Rosalba; Vázquez-Barrientos JC;

PP34 - Clinical, laboratory and glycemic variability profile in a group of T1DM patients attended at a Public University Hospital in the southeast Brazil
Autor(es): Rossi ICB; Rossi BF; Gomes DC; Rodrigues R;

PP35 - Congenital Hyperinsulinism: casuistry report in 10 years of work.
Autor(es): Insúa Beverina MA; Pacheco MGL; Filtrin MR; Tangari A;

PP36 - ENDOTHELIAL DYSFUNCTION AND ATHEROGENIC RISK FACTORS IN ADOLESCENTS WITH TYPE 1 DIABETES MELLITUS.
Autor(es): Valdés W; Espinosa TM; Cabrera JO; Domínguez E;

PP37 - Evaluation of self-care of pediatric diabetic patients followed in an educational program of type 1 diabetes mellitus
Autor(es): Piana MP; Mantovani RM; Villela TR; Canton JMS; Silva IN;

PP38 - Growth assessment in type 1 diabetes mellitus patients attended at the Pediatric Endocrinology Outpatient Clinic of a Federal District Regional Hospital, between 2015 and 2017.
Autor(es): PACHECO NSS; SILVA JM; ALEXANDRE AR; NOGUEIRA JR; BOTELHO NRL; GATTO LRS; RODRIGUES TB; MATSUURA CO; FALLEIROS RKMM; AMORIM BRV; SOUZA JL; TURRA CTD;

PP39 - HNF4A variant causing Congenital Hyperinsulinism: A case report
Autor(es): Gariza AC; La Serna JE;

PP40 - Hyperinsulinemic Hypoglycemia Secondary to Insulinoma in Teenage: Case Report
Autor(es): Schuler TA; Araújo JR; Gomes BGS; Ferreira AHA; Souza KP; Alves KTS; Fernandes ALPR; Gonzalez MMP; Lauro GP; Pereira GCL; Nascimento WE; Andrade MMD;

PP41 - NEONATAL DIABETES MELLITUS RESPONSIVE TO SULPHONYLUREA, DUE TO KCNJ11 MUTATION
Autor(es): ERBES JM; GARCIA TS; LEE JS; CECHINEL E; SIMONI G; NASCIMENTO ML; SILVA PCA;

PP42 - Post-Transplant Diabetes Mellitus in twins with autosomal dominant polycystic kidney disease: A case report
Autor(es): Silva Camarena M.; Calzada León R.; Altamirano Bustamante N.; Arguinzoniz Valenzuela L.; Ruiz Reyes M.; Robles Valdés R.;

PP43 - TYPE 2 DIABETES IN CHILDREN AND ADOLESCENTS: IS IT A REALITY IN SOUTH BRAZIL?
Autor(es): Godinho AM; Dall´Agnese A; Fornari A; Lavigne S; Vissoky GC; Geremia C; Bressiani M; Tschiedel B; Puñales M;

PP45 - Wolfram Syndrome: a cause of monogenic diabetes
Autor(es): ERBES JM; GARCIA TS; LEE JS; CECHINEL E; SIMONI G; NASCIMENTO ML; SILVA PCA;


Genetics

PP47 - Berardinelli Seip Syndrome: Case report
Autor(es): Bergol MFR; Ferragini AA; Cassânego CP; Lima MK; Romão A; Cristovam MAS; Sandrini F;

PP48 - CHARACTERIZATION OF PATIENTS WITH SYNDROME OF MC CUNE ALBRIGHT AND ITS MUTATION OF THE GNSI GENE
Autor(es): Mejia de beldjenna L; Apraez K; Alvarez T; Lammoglia JJ;

PP49 - Familial hypercholesterolemia: a case report
Autor(es): Sales, MTA; Linhares, NPD; Pereira, RABO; Cavalcante, ALVM; Martins, LV; Gonçalves, CS; Sousa, MS; Aragão, LFF; Carvalho, AB; Montenegro, APDR; Gurgel, MHC;

PP50 - Giant cell tumor in a patient with Noonan syndrome
Autor(es): Paulina Schneider; Javiera Basaure; Guillermo Lay-Son; Verónica Palacios; Hugo Cooper;

PP51 - Low frequency of pathogenic allelic variants in the 46,XY differences of sex development (DSD)-related genes in small for gestational age children with hypospadias
Autor(es): Braga BL; Gomes LN; Nishi MY; Freire BL; Batista RL; Funari MFA; Costa EMF; Lerario AM; Domenice S; Junior JADF; Jorge AAL; Mendonca BB;

PP52 - Multiple Hamartoma Syndrome.Presentation of a case from multinodular goiter
Autor(es): Villanueva S; Gárate I; Gallardo V; Yizmeyian A; Rocha A; Sepúlveda C;

PP53 - Novel mutations in the AVP-NPII gene associated with neurohypophyseal diabetes insipidus
Autor(es): Garcia-Castaño A; Madariaga L; Pérez de Nanclares G; Vela A; Rica I; Gaztambide S; Martínez R; Martínez de LaPiscina I; Urrutia I; Aguayo A; Velasco O; Familial neurohypophyseal diabetes insipidus Spanish working group; Castaño L;

PP54 - Screening of c-KIT genetic variants in patients with isolated bilateral cryptorchidism
Autor(es): Rodríguez F; Herrera I; Pieper D; Cassorla F;

PP55 - Variants of Uncertain Significance (“VUS”) in 2 patients with a RASopathie phenotype (Noonan Syndrome)
Autor(es): Arriaza Z. MI; González G. Marcela; Zepeda D.; Rodriguez F;


Pituitary/hypothalamus

PP57 - Classical phenylketonuria about a case
Autor(es): Colmenarez JL; Faria DJ;

PP58 - McCune-Albright Syndrome (MAS) associated with Cushing Syndrome (CS) in a 3-months old infant girl: preliminary results of ketoconazole treatment.
Autor(es): Ferreira R; Lacerda Filho L; Pereira RM; França SN; Demartini AC; Kraemer GC; Carvalho JAR; Bordin L;

PP59 - Metacromatic Leukodistrophy and Central Hypothyroidism, regarding a case
Autor(es): Ramos K;

PP60 - NEAR ADULT HEIGHT ACCORDING TO GENETIC TARGET IN A GIRL WITH MCCUNE ALBRIGHT SYNDROME AND GROWTH HORMONE EXCESS: 12.86 YEARS FOLLOW-UP.
Autor(es): Fernández Mentaberry M V; Riu C.; Oneto A.; Stivel M.;

PP61 - The severity of GH deficiency (GHD) does not affect adherence to treatment in GHD prepubertal children taking rGH via the Easypod device
Autor(es): Loche S;

PP62 - WHEN HAVING TOO MUCH HEIGHT IS A PROBLEM ... A CASE REPORT
Autor(es): López Avellaneda C; Guntsche Z.; Breyer F; Pott Godoy C.; Recabarren A.; Marquez P.; Cuglia N;


Mineral metabolism and vitamin D

PP63 - ADEQUACY OF IRON AND VITAMIN D SUPPLEMENTATION OF CHILDREN BETWEEN ZERO AND TWO YEARS OLD ATTENDED IN A PEDIATRIC AMBULATORY
Autor(es): Vescovi JS; Vescovi ES; Mazzucchetti L; Remor KVT;

PP64 - ATYPICAL PRESENTATION OF VITAMIN D DEPENDENT RICKETS TYPE 1A (VDDR 1A)
Autor(es): Malosetti MC ; Garciarena MA; Vaiani E; Perez Garrido N; Marino R; Belgorosky A;

PP65 - Body mass index presents a strong correlation with Dual X-Ray Absorptiometry-measured adiposity in pediatric patients with Osteogenesis Imperfecta
Autor(es): Pacheco NS; Carlos GA; Chianca LS; Alexandre AR; Silva JM; Oliveira RS; Lopes FSC; Castro LC;

PP66 - Bone evaluation of children and adolescents with Turner Syndrome by quantitative ultrasound of proximal phalanges (QUS)
Autor(es): SALAZAR, KAA; FILGUEIRAS, MFTF; MENDES, LL; CUNHA, SB;

PP67 - Brucks Syndrome, a rare form of Osteogenesis Imperfecta
Autor(es): Garcia TS; Erbes JM; Lee JS; Cechinel E; Simoni G; Nascimento ML ; Silva PCA ;

PP68 - Evaluation of the osteometabolic profile of subjects in the transition phase who were treated with human recombinant growth hormone in childhood. 
Autor(es): Castro ABS; Leone C; Carneiro MS; Damiani D; Kuba VM;

PP69 - Follow up of surgical parathyroidectomy in chronic renal failure patients
Autor(es): Kuspiel Maria Florencia; Troiano Marina; Pasqualini Titania; Alonso Guillermo;

PP70 - Four novel PHEX gene mutations in patients with X-Linked Hypophosphatemia
Autor(es): Silva JM; Alexandre AR; Matsuura CO; Rodrigues TB; Pacheco NSS; Oliveira RS; Lopes FSC; Castro LC;

PP71 - Hypophosphatemic rickets: case report on the diagnosis of rare and variable disease in a family
Autor(es): Jacob CGF; Coelho AP; Villar HCCE; Toreto TMR; Silva LFHF; Ramos LP; Casagrande WM; Borges MM; Amico MMD; Buzzetto AR; Ariosa GZDA;

PP73 - Impact of phosphate and calcitriol supplementation on height and skeletal deformities of patients with X-Linked Hypophosphatemia
Autor(es): Matsuura CO; Rodrigues TB; Pacheco NSS; Alexandre AR; Silva JM; Lopes FSC; Oliveira RS; Castro LC;

PP74 - No difference in the proportion of overweight and obesity among pediatric patients with Osteogenesis Imperfecta throughout a ten-year period
Autor(es): Rodrigues TB; Chianca LS; Carlos GA; Matsuura CO; Silva JM; Alexandre AR; Lopes FSC; Oliveira RS; Castro LC;

PP75 - Parathyroid Adenomas in Pediatrics
Autor(es): Mejia de Beldjenna L; Rodriguez MI; Gomez JF;

PP76 - PHENOTYPE AND GENOTHYPE OF X-LINKED HYPOPHOSPHATEMIC RICKETS IN EIGHT BRAZILIAN CHILDREN AND ADOLESCENTS
Autor(es): Bitencourt BB; Lacerda Filho L ; França SN; Pereira RM; Demartini AC; Kraemer GC; Silvestre L; Carvalho JAR;


Tumors

PP77 - Atypical presentation of prolactinoma in childhood.
Autor(es): Fernandes RGAL; Rossi ISB; Feibelmann TCM; Silva ACAL; Castro SC; Lamberti MO; Gomes DC;

PP78 - Endocrinological effects of cancer and its treatment in childhood
Autor(es): Ferreira LV; Galvão BS; Rezende LM; Machado LD; Ferreira M; Esteves TC;

PP79 - LONG-TERM EVALUATION OF OVARIAN FUNCTION AND FOLLICULAR RESERVE IN PATIENTS WITH MALIGNANT DISEASES TREATED WITH CHEMOTHERAPY IN PREPUBERTAL OR PUBERTAL AGE
Autor(es): Arcari AJ; Freire AV; Grinspon RP; Bedecarrás P; Escobar ME; Ropelato MG; Bergadá IB; Rey RA; Gryngarten MG;

PP80 - Men 1 presentation with insulinoma before 10 years old: case report
Autor(es): Minaberry L; Viale ML; García Minuzzi M; Figueroa Gacitúa V;

PP81 - Peripheral precocious puberty secondary to sexual cord ovarian tumor with annular tubules (TCSTAs) not associated with Peutz-Jeghers syndrome (SPJ)
Autor(es): Garciarena MA ; Rubaja MS ; Vaiani E; Gattari P; Di Matteo E; De La Pía J; Alvarez M; Malosetti MC ;


Obesity

PP82 - Evaluation of Inflammatory Markers, Metabolic Syndrome, hepatic steatosis and measurement of carotid intima in obese juvenile patients
Autor(es): Fernandez Alonso A; Bichara L; Chahla R; Chaila Z; Dupuy M; Elias A; Gines S; Granito S; Graif O; Guerrero C; Simesen G; Bazan C;

PP83 - Evaluation of visceral fat by ultrasound in children and adolescents
Autor(es): Ferreira LV; Piovezan JM; Alvarenga M Q; Rezende LM; Machado LD; Machado IM; Ferreira M; Carmo WB;

PP84 - Hypovitaminosis D in a group of children with obesity and risk of metabolic syndrome.
Autor(es): Menezes CA; Queiroz AS; Vasconcelos RS;

PP85 - IMPACT OF PROBIOTIC THERAPY INTERVENTION ON THE ANTHROPOMETRY OF OBESE CHILDREN AND ADOLESCENTS
Autor(es): Pellicciari CR; Pacheco TL; Artioli TO; Leiderman, DBD; Mimica, MJ; Longui CA; Kochi C;

PP86 - LEVELS OF VITAMIN D AND ITS ASSOCIATION WITH EARLY MARKERS OF CARDIOVASCULAR DISEASE IN CHILDREN AND ADOLESCENTS WITH OVERWEIGHT OR OBESITY
Autor(es): Rodriguez Azrak MS; Klajn DS; Brich TAM; Pipman VR;

PP87 - NUTRITIONAL STATE OF ADOLESCENTS IN THE STATE OF GOIÁS, BRAZIL, IN 2008 AND 2018.
Autor(es): Silva JVP; Nascimento Jr OL; Silva RDCH; Souza CSB; Oliveira LCV; Pinto RM;

PP88 - NUTRITIONAL STATE OF INFANTS UNDER 6 MONTHS OF AGE IN THE STATE OF GOIÁS, BRAZIL, IN 2008 AND 2018
Autor(es): Monteiro GMC; Cavallini LF; Nascimento Jr OL; Oliveira MA; Souza CSB; Pinto RM;

PP89 - NUTRITIONAL STATE OF PRESCHOOL CHILDREN IN THE STATE OF GOIÁS, BRAZIL, IN 2008 AND 2018
Autor(es): Resende RC; Nascimento Jr OL; Oliveira ALV; Freitas PHR; Santos HV; Souza CSB; Pinto RM;

PP90 - Obesity and cardiovascular risk factors in overweight children after at least one year of nutritional intervention
Autor(es): Barreto MCA; Solberg PFC; Gilban DLS; Bordallo AP; Gazolla FM; Assumpção COA; Luz CC; Rodrigues NCP; Oliveira CL; Madeira IR;

PP91 - Prader-Willi Syndrome and Type 2 Diabetes Mellitus
Autor(es): linhares, NPD; Pereira, RABO; Sales, MTAS; Cavalcante, ALVM; Gonçalves, CS; Montenegro, APDR; Carvalho, AB; Sousa, MS; Aragão, LFF;

PP92 - ROHHAD, a rare and challenging syndrome
Autor(es): Garcia TS; Campos Neto MB ; Erbes JM; Lee JS; Cechinel E; Simoni G; Nascimento ML ; Silva PCA;


Others

PP93 - Association between dyslipidemia and Helicobacter pylori infection
Autor(es): Hayes Dorado JP; Eid Lit M; Gorena Montalvo CC; Barbehito Espinoza BK; Herran Cespedes Y;

PP94 - HEMATOCRIT CORRECTION: AN INNOVATIVE TOOL TO REDUCE THE RECALL RATE IN NEWBORN SCREENING OF ENDOCRINOPHATIES
Autor(es): Vilche Juarez A.; Dratler G.; Marino S.; Tommasi F.; Quiroga S.; Coniglio S.; Ciaccio M.;


Puberty e Gender differentiation disorders

PP95 - 5 ALPHA REDUCTASE DEFICIENCY A FAMILY REPORT
Autor(es): POSADAS MENDOZA KJ; BONILLA MEDINA PS; RUIZ REYES ML; CALZADA LEON R; Arguinzoniz Valenzuela L; Bustamante NF ; Robles Valdés C ; Yokoyama Rebollar E; Tapia Hernández B;

PP96 - Anti-Müllerian hormone reference values in paediatric population by electroquimioluminiscence
Autor(es): Ochetti M; Silvano L; Campi V; Sobrero G; Tarifa C; Martin S; Signorino M; Boyanovsky L; Pelliza C; Castro L; Muñoz L; Miras M;

PP97 - Determining factors in the continuity of care in patients with Turner Syndrome during transition.
Autor(es): Alonso G; Troiano M; Fittipaldi Y; Kuspiel MF; Paissan A; Pasqualini T;

PP98 - Development of a LC-MS/MS method to measure simultaneously 10 sexual steroids in Pediatric Endocrinology.
Autor(es): Ambao V; Rodríguez ME; Altube M; Ballerini MG; Bergadá I; Rey RA; Ropelato MG;

PP99 - Diagnostic Challenges in Sex Development Disorders: a Case Report
Autor(es): Klink GA; Lima DM; Steinmetz L; Cominato L; Franco RR; Menezes Filho HC; Della Manna T; Cespedes WCJ; Semer B; Damiani D;

PP100 - Disorders of sexual differentiation experience in the last five years in Mexican children.
Autor(es): Bonilla PS; Posadas KS; Ruiz MDLL; Sletza AV; Calzada R; Altamirano Nelly; Robles C;

PP101 - Evolution of BMI in girls under GnRHa treatment for Idiopathic Central Precocious Puberty.
Autor(es): Rampi MG; Cecchi G; Della Pia B; Fontana ML; Forrester A;

PP102 - Final height evaluation in girls with constitutional early puberty in clinical follow-up.
Autor(es): Jaconis SB; Amendola RM; D‘Souza-Li LFR;

PP103 - Genital abnormalities and pubertal development in a cohort of Prader Willi Syndrome patients
Autor(es): Berbara, HMBL; Beserra, ICR;

PP104 - GnRH analogues treatment: evolution of BMI and body adiposity index
Autor(es): Silva Camarena M.; Calzada León R.; Altamirano Bustamante N.; Arguinzoniz Valenzuela L.; Ruiz Reyes M.; Robles Valdés R.; Orellana Cardenas P.; Vargas Vázquez T.; Silva Camarena MA.;

PP105 - Is ovarian hyperstimulation syndrome in preterm infants a rare entity? Nine patients in four years from one single centre.
Autor(es): Fernandez Mentaberry M V; Bertani G; Riu C; Boichetta G; Otero P; Peisajovich I; Minotti F.; Stivel M;

PP106 - MCCUNE - ALBRIGHT SYNDROME: PHENOTYPE OF PATIENTS TREATED AT A REFERRAL CENTER AND RESPONSE TO KETOCONAZOLE TREATMENT
Autor(es): Ferreira R; Lacerda Filho L; França SN; Pereira RM; Demartini AC; Kraemer GC; Bordin L; Carvalho JAR;

PP107 - OVOTESTICULAR SEXUAL DIFFERENTIATION DISORDER. EXPERIENCE OF THE FEDERICO GÓMEZ CHILDREN‘S HOSPITAL OF MEXICO
Autor(es): Hernández Trejo KE; Martínez Domínguez LG; Baltodano Martínez YV; Elisa Cerón C; Molina Díaz M; Morales Camacho WJ;

PP108 - Partial androgen insensitivity syndrome and phenotypic variation with the same molecular mutation
Autor(es): Gallardo R; Lopez Dacal J; Marino R; Orellano M; Brunetto O; Figueroa Gacitúa V;

PP109 - PERIPHERAL PRECOCIOUS PUBERTY IN A GIRL SECONDARY TO SEX CORD TUMOR WITH ANNULAR TUBULES
Autor(es): Villatoro G; Espinoza LM; Nuñez EA;

PP110 - Precocious central puberty due to an ependymoma, regarding a case
Autor(es): Karen Ramos Rodríguez;

PP111 - Puberty in patients with Ovotesticular DSD: evaluation of 20 patients
Autor(es): Melardi JW; Cunha DFS; Cespedes WCJ; Carvalho FM; Cominato L; Menezes Filho HC; Manna TD; Franco RR; Semer B; Steinmetz L; Damiani D; Castro ABS;

PP112 - RARE VARIANTS of TURNER SYNDROME: clinical presentation and cytogenetics in two cases.
Autor(es): Insúa Beverina MA; Arias Cau AC; Huidobro Ruiz P; Martinez Taibo C; Salim E; Hernandez SC; Nader JF;

PP113 - Sexual mosaisisms. Case report
Autor(es): Espinosa RT; Valdés GW; López PH; Leyva GG;

PP114 - Testicular Macrophage Subpopulations in Androgen Insensitivity Syndrome
Autor(es): Berensztein E; Rivarola MA ; Belgorosky A;

PP115 - Vaginal Endodermal Sinus Tumor (Yolk Sac Tumor) And Premature Thelarche Simulating A Precocious Puberty: A Case Report
Autor(es): Novaes ACL; Miranda Neto LFR; Rocha IN; Parente IX; Carvalho CAS; Rosales FHD; Ribeiro IM; Costa AN; Silva GTO;


Thyroid

PP116 - A novel mutation in the thyroid hormone receptor β gene in a patient who developed thyroid nodules
Autor(es): Hidalgo Coronado L; Chamoux A; Brunetto O; Bre M; Laham M; Adrover E; Molina M; Rivolta CM;

PP117 - Antithyroid drug treatment in children and teenagers with Graves’ disease
Autor(es): Vasconcellos GL; Beserra ICR;

PP118 - Congenital Hypothyroidism screening program: experience with a TSH lower cutoff in Buenos Aires City.
Autor(es): Vieites A.; Enacan R; Ropelato MG; Gotta G; Dratler G; Junco M; Maccalini G; Micenmacher V.; Aranda C; Chiesa A;

PP119 - Conversion of hypothyroidism by Hashimoto’s Thyroiditis (HT) to hyperthyroidism due to Graves Disease (GD) in a previously healthy child
Autor(es): Costa AP; Fochi, CC; Ali, FR; Ferreira, JCG; Pimentel, SS; Pimentel, SS; Soares,GJB;

PP120 - Differential diagnosis of hepatitis in the course of methimazole treatment.
Autor(es): Pires JVG; Miranda RD; Borges IC; Gomes DC;

PP121 - Differentiated thyroid carcinoma in children and adolescents: Clinical presentation, ATA risk-classification and prognosis
Autor(es): Camassola B; Maccarini J; Caciatori J; Geremia C; Gonçalves I; Puñales M;

PP122 - Diffuse sclerosing variant of papillary thyroid carcinoma, a cause of goitre in a pediatric patient
Autor(es): López LA; Sangri RE; Lopez Perez D.; Benitez FJ; Meixueiro CC; Contreras CV; Gallardo JM;

PP123 - Efficacy of levothyroxine on the frequency and severity of migraine in children with subclinical hypothyroidism
Autor(es): Hayes Dorado JP; Flores Rafael G; Justiniano Vargas G; Quispe Morrore D; Totola Colque DM;

PP124 - Establishment of Reference Intervals for thyrotropin, thyroxine, free thyroxine and triiodothyronine in neonates and infants.
Autor(es): Rodriguez MP; Sobrero GM; Campi V; Martin S; Silvano L; Tarifa C; Testa G; Alloza P; Beltran F; Dichko D; Ochetti M; Muñoz L; Miras M;

PP125 - Follow up of pediatrics patients with Graves Basedow Disease.
Autor(es): Calagua M.; DelAguila C.; Lu R.; Nuñez O.; Chavez E.; Espinoza O.; Pinto P.; DelosSantos M.;

PP126 - HEMITHYROIDECTOMY IN A PEDIATRIC COHORT: THYROID FUNCTION FOLLOW UP
Autor(es): Papendieck P; Masnata ME; Bergada I; Chiesa A;

PP127 - Hypoparathyroidism After Thyroid Surgery: Results From The Mexican Population Registry between 2012-2019
Autor(es): Isabel Galán; Lucia Reyes; Calzada Raul; Arguinzoniz Lissette; Ruiz Maria de la Luz; Diaz Luisa; Hinojosa Carlos;

PP128 - Intrathyroidal ectopic thymus mimicking thyroid nodules in children
Autor(es): Munoz T; De Tezanos-Pinto, A; Moenne K; Ortega X; Hernandez MI;

PP129 - Late diagnosis congenital hypothyroidism and abnormal activity of alpha-L Iduronidase (IDUA)
Autor(es): Mendiola M;

PP130 - Methimazole therapy outcomes in pediatric hyperthyroidism
Autor(es): Ricci J; Morín A; Moreno MR; García Rusca EL; Francesca JS; González VG; Tournier A; Fasano MV; Balbi VA;

PP131 - MUTATION OF THE THYROID HORMONE RECEPTOR AS A CAUSE OF RESISTANCE TO THYROID HORMONE.CASE REPORT
Autor(es): Faries S; Alvarez T; Mejia de Beldjenna L;

PP132 - Mutations in Thyroid Hormone Beta Receptor Gene Identified in Children with Clinical Resistance to Thyroid Hormones
Autor(es): González V.; Balbi V.; Morin A; Reinoso A; Vitale L; Ricci J; Espósito M; Martin R; Tournier A; Adrover E; Molina M; Targovnik H; Rivolta C;

PP133 - NEONATAL SCREENING PROGRAM IN THE CITY OF SANTA CRUZ, BOLIVIA, 10 YEARS OF EXPERIENCE
Autor(es): B. Seoane; C.Siva;

PP134 - Newborn of mothers with Graves´ disease: a case series
Autor(es): Irazusta F; Pintado M; Vidal F; Finozzi MR; Rodriguez MN; Blasina F; Sobrero H; Mendoza B;

PP137 - PATIENT’S PROFILE CHARACTERIZATION OF DOWN SYNDROME AND CONGENITAL HYPOTHYROIDISM IN A NEONATAL SCREENING PROGRAM IN SOUTHERN BRAZIL
Autor(es): Rizzotto MIB; Frez DCL; Carreiro S; Vargas PR; Garcia RMR; Castro SM; Kopacek C;



Oral Presentation Finalists (in english)

OPF1 - Loss-of-function NNT mutations impair antioxidants mechanisms and decreases adrenal steroids secretion in patients with familial glucocorticoid deficieny (FGD)
Autor(es): Bodoni AF; Coeli-Lacchini FB; Sobral LM; Moreira AC; Castro M; Leoplodino AM ; Antonini SR;

OPF2 - MAPK8 activation partially compensates the effects of NNT deficiency in adrenocortical cells
Autor(es): Gebenlian, JL; Bodoni, AF; Coeli-Lacchini, FB; Antonini, SR;

OPF3 - Clinical and genetic aspects of pediatric pheochromocytomas and paragangliomas
Autor(es): Guimaraes AG; Petenuci J; Benedetti AF; Fagundes GFC; Pereira MA; Zerbini MN; Yamauchi F; Srougi V; Tanno FY; Chambo JL; Latronico AC; Mendonca BB; Fragoso MB; Almeida MQ;

OPF4 - Risk alleles of FTO, DRD2 and ANKK1 genes are associated with metabolic risk and have an additive effect on childhood obesity outcome.
Autor(es): Pinto RM; Fortes JS; Monteiro RV; Curado MP; Minasi LB; da Cruz, AD;

OPF5 - T2DRIVE as a new MRI protocol for the diagnosis of Pituitary stalk interruption syndrome (PSIS).
Autor(es): Vieira Peixoto G; Lyra A; Nunes ACB; Gurjão M; Silva TS; Meira AS; Rocha AJ; Longui C; Kochi C;

OPF6 - SEXUAL DIMORPHISM IN THE ASSOCIATION OF BMI TRAJECTORY FROM BIRTH TO EARLY ADULTHOOD WITH CARDIOMETABOLIC RISK IN ADULTHOOD: AN APPROACH USING DYNAMIC PROGRAMMING
Autor(es): CORREA-BURROWS P; ROGAN J; BUNOUT D; BARRERA G; BLANCO E ; GAHAGAN S; BURROWS R;

OPF7 - VALIDITY ASSESSMENT OF THE SINGLE-POINT INSULIN SENSITIVITY ESTIMATOR (SPISE) FOR DIAGNOSIS OF CARDIOMETABOLIC RISK IN 16 YEARS-OLD MALE AND FEMALE ADOLESCENTS.
Autor(es): CORREA-BURROWS P; BLANCO E; GAHAGAN S; BURROWS R;

OPF8 - Burosumab resulted in greater improvement in clinical outcomes than continuation with conventional therapy in younger (1-4 years-old) and older (5-12 years-old) children with X-linked hypophosphatemia (XLH)
Autor(es): Ward LM; Imel EA; Skrinar A; San Martin J;

OPF9 - Clinical and Genetic Characterization of a Constitutional Delay of Growth and Puberty Cohort
Autor(es): Barroso PS; Jorge AAL; Lerario AM; Montenegro LR; Lima-Amato LG; Vasques GA; Silveira LFG; Mendonca BB; Latronico AC;

OPF10 - Predictive Factors, Clinical Characteristics, Reproductive hormones and Growth Factors During Pubertal Transition in Girls with Transient Thelarche
Autor(es): SOTO B. J; MERICQ V.; PEREIRA A.; BUSCH AS; ALMSTRUP K.; Corvalan C.; Juul A.;



Poster Presentation Finalist

PPF1 - Cardio-metabolic risk factors in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Autor(es): Espinosa RT; Valdés GW; Cabrera RJO; Domínguez AE; Pesantez KA; Cordero MD;

PPF2 - EHLERS-DANLOS SYNDROME: MOLECULAR AND CLINICAL CHARACTERIZATION OF TNXA/TNXB CHIMERAS IN CONGENITAL ADRENAL HYPERPLASIA PATIENTS
Autor(es): Marino R; Notaristéfano G; Perez Garrido N; Ramirez P; Touzon MS; Pujana M; Moresco A; Vaiani E; Finkielstain G; Obregón G; Balbi V; Rivarola MA; Belgorosky A;

PPF3 - Synchronization ontogeny between adrenal steroidogenesis genes and circadian rhythm of corticosterone secretion in rats.
Autor(es): Brufatto, J P T; Roa SLR; Antonini SR; Martins CS; Bueno AC; Mermejo LM; Moreira AC;

PPF4 - Response to growth hormone in very young children (<2 years) with growth hormone deficiency compared with prepubertal children aged ≥2 years: data from the NordiNet® International Outcome Study and ANSWER Program
Autor(es): Rohrer T; Ostrow V; Pietropoli A; Berger M; Polak M; Ross J;

PPF5 - IMPACTS ON THE USE OF ZOLEDRONIC ACID IN PATIENTS WITH DIAGNOSIS OF OSTEOGENESIS IMPERFECTA EXPERIENCE IN 18 YEARS.
Autor(es): Orellana-Cárdenas P; Calzada-León R.; Robles-Valdés C.; Altamirano-Bustamante N.; Arguinzoniz-Valenzuela L.; Ruiz-Reyes M; Silva-Camarena M.; Díaz- García L.; Bonilla-Medina P.; Maqueda- Tenorio S.;

PPF6 - CALCITRIOL AS A POTENTIAL THERAPEUTIC OPTION FOR THE TREATMENT OF LEYDIG CELL TUMORS
Autor(es): VARELA ML; ABIUSO AMB; BESIO MORENO M; PIGNATARO OP; BELGOROSKY A; BERENSZTEIN E; MONDILLO C;

PPF7 - BODY MASS INDEX INFLUENCE ON POSTURE OF CHILDREN AND ADOLESCENTS: A BIOPHOTOGRAMMETRY ANALYSIS.
Autor(es): LIMA PLM; Breziniscki MP; Pedrassoli GH; Lacerda Filho L; França SN; Pereira RM; Demartini AC; Kraemer GC; RADOMINSKI RB; FORLIN RB; Carvalho JAR;

PPF8 - NUTRITION, RATHER THAN ETHNICITY AND SOCIOECONOMIC STATUS, CORRELATES WITH AGE OF MENARCHE IN AMAZONIAN GIRLS
Autor(es): Oliveira KC; Antonini SRR; Aragon DC; Cardoso Neto J;

PPF9 - Usefulness of Doppler assessment of the uterine artery for the diagnosis of early sexual development in girl
Autor(es): Silva EFF; Antunes JMV; Antunes OAV; Lima MLLC; Cunha SB; Filgueiras MFTF; Silva IN;

PPF10 - Genetic syndrome and congenital hypothyroidism: profile analysis of patients diagnosed in a neonatal screening reference service after reduction of TSH filter cutoff
Autor(es): Carreiro S; Rizzotto MIB; Garcia RMR; Frez DCL; Castro SM; Kopacek C;






Venue

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Address: Rodovia Vereador Onildo Lemos, 2505 - Santinho - Florianópolis / SC / BRASIL
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