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