Familial hyperreninemic hypoaldosteronism type 2: Difference between revisions
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(Created page with "__NOTOC__ {{SI}} {{CMG}} {{SK}} Aldosterone synthase deficiency unlinked to CYP11B2; aldosterone synthase deficiency unlinked to the aldosterone synthase gene; FHHA2. ==Over...") |
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==Overview== | ==Overview== | ||
Familial hyperreninemic hypoaldosteronism type 2 is a very rare genetic disorder which results in a deficiency of aldosterone. The condition can be severe enough to cause infant death unless the patient is diagnosed and treated.<ref name="pmid11701710">{{cite journal |author=Kayes-Wandover KM, Tannin GM, Shulman D, Peled D, Jones KL, Karaviti L, White PC |title=Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene |journal=[[The Journal of Clinical Endocrinology and Metabolism]] |volume=86 |issue=11 |pages=5379–82 |year=2001 |month=November |pmid=11701710 |doi= |url=http://jcem.endojournals.org/cgi/pmidlookup?view=long&pmid=11701710 |accessdate=2012-08-11}}</ref> | |||
==Refernces== | ==Refernces== |
Latest revision as of 00:54, 12 August 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Aldosterone synthase deficiency unlinked to CYP11B2; aldosterone synthase deficiency unlinked to the aldosterone synthase gene; FHHA2.
Overview
Familial hyperreninemic hypoaldosteronism type 2 is a very rare genetic disorder which results in a deficiency of aldosterone. The condition can be severe enough to cause infant death unless the patient is diagnosed and treated.[1]
Refernces
- ↑ Kayes-Wandover KM, Tannin GM, Shulman D, Peled D, Jones KL, Karaviti L, White PC (2001). "Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene". The Journal of Clinical Endocrinology and Metabolism. 86 (11): 5379–82. PMID 11701710. Retrieved 2012-08-11. Unknown parameter
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