17 alpha-hydroxylase deficiency causes: Difference between revisions

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{{Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency}}
{{17 alpha-hydroxylase deficiency}}
{{CMG}}; {{AE}} {{Ammu}}
{{CMG}}; {{AE}}, {{MJ}}
 
==Overview==
==Overview==
Mutations in the ''[[CYP17A1]]'' gene cause congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency.
Mutations in the [[CYP17A1]] [[gene]] cause 17 alpha-hydroxylase deficiency. This [[gene]] is located on [[chromosome]] 10.
==Causes==
==Causes==
Mutations in the ''[[CYP17A1]]'' gene cause congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency.<ref> Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency. Wikipedia (2016). https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_17_alpha-hydroxylase_deficiency Accessed on January 29, 2016</ref>
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}}
[[Category:Disease]]
[[Category:Pediatrics]]
[[Category:Endocrinology]]
[[Category:Genetic disorders]]
[[Category:Intersexuality]]

Latest revision as of 16:20, 20 October 2017

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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

  1. 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.