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.
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| Main Authors: | , |
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| Format: | Book |
| Published: |
Indonesian Pediatric Society Publishing House,
2019-09-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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