C-11 Hydroxylase Deficiency: eMedicine Endocrinology
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C-11 Hydroxylase Deficiency: eMedicine Endocrinology
Overview: Congenital adrenal hyperplasia (CAH) is a general term used to describe a group of inherited disorders in which a defect in cortisol biosynthesis is present with consequent overproduction of adrenocorticotropic hormone (ACTH) and secondary adrenal hyperplasia ...
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Tags: Endocrinology, Hormone, Disease and Condition, Childbirth
Most Recently Shared on May 5, 2010 at 6:16 pm By:
The prevalence of C-11 hydroxylase deficiency is approximately 1 case per 100,000 live births. Learn more. http://bit.ly/dpfa1h
C-17 Hydroxylase Deficiency: eMedicine Endocrinology
emedicine.medscape.com — “Overview: The rare variant of congenital adrenal hyperplasia (CAH) known as 17-hydroxylase deficiency was first described in the 1960s in patients with sexual infantilism and hypertension. It has also been described to present in the setting of ...” View full resource at emedicine.medscape.com
Most Recently Shared on May 5, 2010 at 6:25 pm By:
C-17 hydroxylase deficiency is reportedly very rare, with less than 150 well-validated cases documented. Learn more. http://bit.ly/crAjxZ
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