𝔖 Bobbio Scriptorium
✦   LIBER   ✦

DETECTION OF HETEROZYGOTE OF 21-HYDROXYLASE DEFICIENCY

✍ Scribed by Levine, LenoreS.; Pang, Songja; Dupont, Bo; Pollack, Marilyn; Lorenzen, Franziska; New, MariaI.


Book ID
123256032
Publisher
The Lancet
Year
1980
Tongue
English
Weight
311 KB
Volume
315
Category
Article
ISSN
0140-6736

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Identification of heterozygotic carriers
✍ Witchel, Selma F.; Lee, Peter A. πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 37 KB πŸ‘ 1 views

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency is a common autosomal-recessive disorder. To ascertain carrier status, adrenocorticotropin (ACTH) stimulation tests are often used. To determine the sensitivity of ACTH stimulation to detect heterozygotes and to correlate stimulated 17-