## Abstract Steroid 11β‐hydroxylase deficiency is relatively frequent in Israel among North African Jews. Over a 39‐year period, 38 affected individuals from 25 families were diagnosed. Nineteen families came from Morocco, and in another 2, one parent came from Morocco (80% of all parents). Demogra
✦ LIBER ✦
Virilizing adrenal tumour mimicking congenital adrenal hyperplasia with P450c11 (11β-hydroxylase) deficiency
✍ Scribed by E. A. Werder; R. Voutilainen; M. Zachmann
- Publisher
- Springer
- Year
- 1994
- Tongue
- English
- Weight
- 610 KB
- Volume
- 153
- Category
- Article
- ISSN
- 0340-6997
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
High frequency of congenital adrenal hyp
✍
Rösler, Ariel ;Leiberman, Esther ;Cohen, Tirza
📂
Article
📅
1992
🏛
John Wiley and Sons
🌐
English
⚖ 744 KB
Leydig cell tumor in two brothers with c
✍
Pegah Entezari; Abdol Mohammad Kajbafzadeh; Fatemeh Mahjoub; Mohammad Vasei
📂
Article
📅
2011
🏛
Springer Netherlands
🌐
English
⚖ 296 KB
Genotype of Yupik Eskimos with congenita
✍
Phyllis W. Speisere; Maria I. New; Grace M. Tannin; Donald Pickering; Soo Young
📂
Article
📅
1992
🏛
Springer
🌐
English
⚖ 266 KB
HLA Typing of Patients with 21-Hydroxyla
✍
Mohammad Taghi Haghi Ashtiani; Ali Rabbani; Fereidoun Mostafavi; Maryam Monajemz
📂
Article
📅
2008
🏛
Springer
🌐
English
⚖ 155 KB
Substitution of Ile-172 to Asn in the st
✍
Jukka Partanen; R. Duncan Campbell
📂
Article
📅
1991
🏛
Springer
🌐
English
⚖ 543 KB
The steroid 21-hydroxylase enzyme (P450c21) is a member of the cytochrome P450 gene superfamily and is essential in the synthesis of cortisol and aldosterone. Defects in the P450c21B gene cause congenital adrenal hyperplasia (CAH), a common genetic disorder leading to virilization of newborn females
Sharing of MHC haplotypes among apparent
✍
Z. Layrisse; C. White; P. Gunczler; L. Gafaro Valera; S. Arias; E. J. Yunis; C.
📂
Article
📅
1987
🏛
Springer-Verlag
🌐
English
⚖ 481 KB