hrp0098p3-346 | Late Breaking | ESPE2024

Severe Adolescent Androgenization secondary to an Ectopic Hilus Cell Nodule: a Case Report

Dey Subrata , Samaddar Sukla

Introduction: Virilization and menstrual irregularities in a background of insulin resistance in adolescents is commonly attributed to polycystic ovarian disease (PCOD). However, clinicians should have a high index of suspicion for causes masquerading as PCOD when encountering atypical findings. We describe a case where we identified a rare cause of androgen excess.Case: A 13-year-old girl presented with primary amenorrh...

hrp0098p2-297 | Late Breaking | ESPE2024

CYP21A2 genotype and phenotypic manifestation in children with congenital adrenal hyperplasia from a tertiary care center in Eastern India.

Samaddar Sukla , Dey Subrata , Raj Neethu , Correa Alec

Introduction: Genetic mutation in the CYP21A2 gene presents with various phenotypes in congenital adrenal hyperplasia (CAH). We conducted a cross-sectional study of the genotypic pattern and its corresponding phenotype at a tertiary care hospital of Eastern India.Method: We screened all children aged between 0-18 years under follow-up who underwent genetic analysis for CYP21A2 mutations based on clinical or biochemical f...