No Linkage between HLA and Congenital Adrenal Hyperplasia Due to 11-β-Hydroxylase Deficiency
- 25 January 1979
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 300 (4) , 205-206
- https://doi.org/10.1056/nejm197901253000433
Abstract
To the Editor: The various forms of congenital adrenal hyperplasia are caused by different enzymatic deficiencies, each responsible for a given step in the biosynthesis of cortisol or aldosterone (or both). The most frequent forms of this disorder result from deficiencies of the 21-hydroxylase and 11-hydroxylase enzymes.1 These enzymes function sequentially in steroid biosynthesis and therefore may be genetically linked, similar perhaps to the lactose system in Escherichia coli.2 Since close genetic linkage between congenital adrenal hyperplasia, 21-hydroxylase deficiency and the B locus of the HLA system has recently been shown,3 4 5 it was of interest to determine if the . . .Keywords
This publication has 5 references indexed in Scilit:
- HLA AND CONGENITAL ADRENAL HYPERPLASIA LINKAGE CONFIRMEDThe Lancet, 1978
- CLOSE GENETIC LINKAGE BETWEEN HLA AND CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY)The Lancet, 1977
- Congenital Adrenal HyperplasiaPublished by Springer Nature ,1973
- Enzymatic Mechanism of Steroid HydroxylationScience, 1969
- HYDROXYLATION OF STEROIDS AT CARBON 21Journal of Biological Chemistry, 1957