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Congenital adrenal hyperplasia. Plasma and urinary steroid conjugates in seven children with steroid 21-hydroxylase deficiency

✍ Scribed by L. Viinikka; O. Jänne; J. Perheentupa; R. Vihko


Book ID
115820083
Publisher
Elsevier Science
Year
1973
Tongue
English
Weight
660 KB
Volume
48
Category
Article
ISSN
0009-8981

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A rapid screening for steroid 21-hydroxy
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Steroid 21-hydroxylase deficiency is the major cause of congenital adrenal hyperplasia (CAH). CAH due to 21-hydroxylase deficiency is divided into three classes: salt-wasting (classical), non-classical and simple virilizing, reflecting different degrees of clinical severity. Using polymerase chain r