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Insulin sensitivity and body composition in children with classical and nonclassical congenital adrenal hyperplasia

✍ Scribed by R. M. Williams; A. Deeb; K. K. Ong; W. Bich; P. R. Murgatroyd; I. A. Hughes; C. L. Acerini


Book ID
108704456
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
91 KB
Volume
72
Category
Article
ISSN
0300-0664

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Classical congenital adrenal hyperplasia (CAH) results from an inherited enzymatic defect in cortisol synthesis and more than 90 per cent of cases are due to 21-hydroxylase deficiency. The androgen excess associated with this condition typically results in ambiguous external genitalia in affected fe