17 alpha-hydroxylase deficiency causes: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
Iqra Qamar (talk | contribs) |
||
| (3 intermediate revisions by one other user not shown) | |||
| Line 1: | Line 1: | ||
__NOTOC__ | __NOTOC__ | ||
{{ | {{17 alpha-hydroxylase deficiency}} | ||
{{CMG}}; {{AE}} {{ | {{CMG}}; {{AE}}, {{MJ}} | ||
==Overview== | ==Overview== | ||
Mutations in the | Mutations in the [[CYP17A1]] [[gene]] cause 17 alpha-hydroxylase deficiency. This [[gene]] is located on [[chromosome]] 10. | ||
==Causes== | ==Causes== | ||
Mutations in the | Mutations in the [[CYP17A1]] [[gene]] cause 17 alpha-hydroxylase deficiency. This [[gene]] is located on [[chromosome]] 10.<ref name="pmid4288776">{{cite journal |vauthors=Biglieri EG, Herron MA, Brust N |title=17-hydroxylation deficiency in man |journal=J. Clin. Invest. |volume=45 |issue=12 |pages=1946–54 |year=1966 |pmid=4288776 |pmc=292880 |doi=10.1172/JCI105499 |url=}}</ref> | ||
==Reference== | ==Reference== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Latest revision as of 16:20, 20 October 2017
|
17 alpha-hydroxylase deficiency Microchapters |
|
Differentiating 17 alpha-hydroxylase deficiency from other Diseases |
|
Diagnosis |
|
Treatment |
|
Case Studies |
|
17 alpha-hydroxylase deficiency causes On the Web |
|
American Roentgen Ray Society Images of 17 alpha-hydroxylase deficiency causes |
|
Risk calculators and risk factors for 17 alpha-hydroxylase deficiency causes |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: , Mehrian Jafarizade, M.D [2]
Overview
Mutations in the CYP17A1 gene cause 17 alpha-hydroxylase deficiency. This gene is located on chromosome 10.
Causes
Mutations in the CYP17A1 gene cause 17 alpha-hydroxylase deficiency. This gene is located on chromosome 10.[1]
Reference
- ↑ Biglieri EG, Herron MA, Brust N (1966). "17-hydroxylation deficiency in man". J. Clin. Invest. 45 (12): 1946–54. doi:10.1172/JCI105499. PMC 292880. PMID 4288776.