A paradox: Elevated 21-hydroxypregnenolone production in newborns with 21-hydroxylase deficiency
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry
Reference32 articles.
1. The Investigation of Steroid Metabolism in Early Infancy
2. STEROID EXCRETION PATTERNS IN URINE FROM TWO BOYS IN THE NEONATAL PERIOD WITH CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY
3. Identification of 15β-hydroxylated c21 steroids in the neo-natal period: The role of 3α, 15β,17α-trihydroxy-5β-pregnan-20-one in the perinatal diagnosis of congenital adrenal hyperplasia (cah) due to a 21-hydroxylase deficiency
4. Inborn errors of steroid biosynthesis.
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