hrp0098p3-236 | Sex Differentiation, Gonads and Gynaecology, and Sex Endocrinology | ESPE2024
Diab Dina
, Alaa El-Din Thabet Mohammed
, Marzouq Iman
, Elneely Dalia
, Tawfeeq Soliman Ashraf
, Elawwa Ahmed
, Elsayed Shymaa
Background: Congenital Adrenal Hyperplasia (CAH) is characterized by various enzyme deficiencies, notably 11-Beta-Hydroxylase Deficiency (11OHD) and 21-Hydroxylase Deficiency (21OHD), each affecting growth and hormonal levels differently. This study aim ed to compare the anthropometric and hormonal profiles of pediatric patients affected by these two conditions.Methods: The clinical records of pediatric patients diagnose...