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Biochemical Basis for the Manifestations of Iron Deficiency

โœ Scribed by Dallman, P R

Book ID
115481491
Publisher
Annual Reviews
Year
1986
Tongue
English
Weight
674 KB
Volume
6
Category
Article
ISSN
0199-9885

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The biochemical basis for genotyping 21-
The biochemical basis for genotyping 21-hydroxylase deficiency
โœ Maria I. New; Bo Dupont; Marilyn S. Pollack; Lenore S. Levine ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› Springer ๐ŸŒ English โš– 366 KB

We describe three different forms of 21-hydroxylase deficiency-classical congenital adrenal hyperplasia (CAH), late-onset 21-hydroxylase deficiency, and cryptic 21-hydroxylase deficiency-and we present hormonal standards by which to assign the appropriate 21-hydroxylase deficiency genotype for these