SCREEN 1:                      

146: PERSISTENT MÜLLERIAN DUCT SYNDROME: REMAINING PITFALLS IN THE DIAGNOSIS AND THE ROLE OF CLOSE MONITORING IN A TERTIARY CENTRE | Dsd Adrenal

189: HYPOGONADOTROPIC HYPOGONADISM WITH BILATERAL CRYPTORCHIDIA: CASE PRESENTATION | Dsd Adrenal

94: CHARACTERIZATION OF PATIENTS DIAGNOSED WITH UTERINE ANOMALIES IN A PEDIATRIC INSTITUTION FOR THE PERIOD 2008 TO 2023 | Gynecology

37: SOCIODEMOGRAPHIC AND CLINICAL CHARACTERIZATION OF PEDIATRIC PATIENTS DIAGNOSED WITH SICKLE CELL ANEMIA WITH ENDOCRINOPATHIES IN A PUBLIC HOSPITAL IN CALI-COLOMBIA   2017 – 2022 | Oncology

82: ENDOCRINE MANIFESTATIONS IN AN ADOLESCENT GIRL WITH CARNEY COMPLEX | Oncology

SCREEN 2:      

163: SEVERE HYPERINSULINC HYPOGLYCEMIA AS THE FIRST MANIFESTATION OF MEN1 IN A 7 YEAR–OLD CHILD

116: CLINICAL, ANTHROPOMETRIC AND LABORATORY DATA OF GIRLS WITH PRECOCIOUS PUBERTY BEFORE, DURING AND AFTER COVID-19 PANDEMIC LOCKDOWN.

185: INTERNATIONAL SURVEY OF MEDICAL MANAGEMENT TO RESTORE MINI-PUBERTY FOR MALE INFANTS WITH CONGENITAL HYPOGONADOTROPIC HYPOGONADISM (CHH) –  A MULTICENTER INTERNATIONAL ENDEAVOUR TO OPTIMIZE REPRODUCTIVE OUTCOMES

32: CHARACTERIZATION OF PATIENTS WITH KLINEFELTER'S SYNDROME IN A LEVEL IV PEDIATRIC INSTITUTION

145:      ESTUDIO DESCRIPTIVO DE LA EDAD DE LA MENARCA A 3625 MSNM LA PAZ – BOLIVIA 2022

SCREEN 3:      

126: SEPTO-OPTIC DYSPLASIA DUE TO SOX2 MUTATION. CASE REPORT.

33: FAMILIAL NEUROHYPOPHYSEAL DIABETES INSIPIDUS CAUSED BY A NOVEL MUTATION IN AVP-NPII GENE IN TWO PERUVIAN BROTHERS

127: CENTRAL DIABETES INSIPIDUS WITH FAMILIAL PRESENTATION, A CASE REPORT

49: UN UNUSUAL PITUITARY TUMOR

SCREEN 4:      

191: ABSENT MRI NEUROHYPOPHYSIAL BRIGHT SIGNAL IN A TODDLER WITH AVP RESISTANCE

195: THYROID HORMONE RESISTANCE SYNDROME ASSOCIATED WITH MUTATION IN THE SLC16A2 GENE: AN ALLAN-HERNDON-DUDLEY-SYNDROME CASE REPORT

129: HYPERTHYROIDISM IN PEDIATRIC DOWN SYNDROME PATIENTS

35: CHARACTERIZATION OF ECTOPIC THYROID IN PEDIATRIC PATIENTS: CASE SERIES

83: FOLLOWUP OF SUBCLINICAL HYPOTHYROIDISM IN A GROUP OF CHILDREN DURING TWO YEARS

SCREEN 5:      

56: CASE REPORT OF HYPERLIPOPROTEINEMIA IN A PEDIATRIC PATIENT HOMOZYGOUS FOR APOC2 DEFICIENCY AND LCAT DEFICIENCY.

61: 46,XX OVOTESTICULAR SEX DIFFERENTIATION DISORDER (DSD) WITH HETEROZYGOUS VARIANT IN THE DMRT1 GENE: EVALUATION AND MANAGEMENT.

68: FRONTOMETAPHYSEAL DYSPLASIA TYPE II, A DIFFERENT PRESENTATION ASSOCIATED WITH A NEW MISSENSE VARIANT IN MAP3K7. CASE REPORT.

96: VIRILIZATION IN UTERO SECUNDARY TO A MATERNAL KRUKENBERG TUMOR

125: BEYOND THE PHENOTYPE. CASE REPORT OF 3 PATIENTS WITH NON-TYPICAL NOONAN SYNDROME (NS)