hrp0097p2-76 | Adrenals and HPA Axis | ESPE2023
Yang Haihua
, Wei Haiyan
, Huang Ai
, Chen Yongxing
, Li Yangshiyu
Purpose: Identify CYP21A2 gene variants in pediatric patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency from Henan, China, and to analyze genotype-phenotype correlations. We also analyze the relationship between the clinically effective dosage of hydrocortisone and CYP21A2 genotype.Materials/Methods:A total of 214 21-OHD children were recruited in Henan children's hospital from 2008 to 202...