Congenital Adrenal Hyperplasia (Case Report)
Abstract
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.
References
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Published 2019-09-18