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Cognitive functioning in female patients with 21-hydroxylase deficiency

✍ Scribed by Ralf W. Dittmann; Michael H. Kappes; Marianne E. Kappes

Publisher
Springer
Year
1993
Tongue
English
Weight
721 KB
Volume
2
Category
Article
ISSN
1018-8827

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## Abstract Steroid 21‐hydroxylase deficiency is present in more than 90% of patients with congenital adrenal hyperplasia (CAH), an inherited metabolic disorder of adrenal steroidogenesis. Impaired enzymatic activity leads to the accumulation of metabolic intermediates (progesterone and 17‐hydroxyp