In:
Journal of the Bahrain Medical Society, HealthMinds Consulting Pte Ltd, Vol. 25, No. 2 ( 2022), p. 108-111
Kurzfassung:
Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder commonly caused by 21-hydroxylase deficiency. It accounts for 90-95% of cases. The second most common cause is 11β hydroxylase deficiency. We report on the first case of 11β hydroxylase deficiency in Bahrain with a review of the literature.
Materialart:
Online-Ressource
ISSN:
1015-6321
,
2960-6004
DOI:
10.26715/jbms.25_2_11
Sprache:
Unbekannt
Verlag:
HealthMinds Consulting Pte Ltd
Publikationsdatum:
2022