Congenital Adrenal Hyperplasia (Case Report)

A case of a female infant with congenital abnormality of the urogenital apparatus, an excess of the urinary 17-ketosteroid, mild salt losing disorder, acceleration of growth ossification, described as congenital adrenal hyperplasia due to 21-hydroxylase defect has been reported.

Bibliographic Details
Main Authors: Marwoto Marwoto, Achmad Surjono
Format: Article
Language:English
Published: Indonesian Pediatric Society Publishing House 2019-09-01
Series:Paediatrica Indonesiana
Subjects:
Online Access:https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/2315