17 alpha-hydroxylase deficiency causes: Difference between revisions
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Mutations in the ''CYP17'' gene cause congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. | Mutations in the ''CYP17'' gene cause congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. | ||
==Causes== | ==Causes== | ||
Mutations in the ''CYP11B1'' gene cause congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.<ref> Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. Wikipedia (2016). https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_11%CE%B2-hydroxylase_deficiency Accessed on January 29, 2016</ref> | |||
==Reference== | ==Reference== | ||
{{Reflist|1}} | {{Reflist|1}} | ||
Revision as of 19:45, 7 February 2016
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Congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
Mutations in the CYP17 gene cause congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.
Causes
Mutations in the CYP11B1 gene cause congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.[1]
Reference
- ↑ Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. Wikipedia (2016). https://en.wikipedia.org/wiki/Congenital_adrenal_hyperplasia_due_to_11%CE%B2-hydroxylase_deficiency Accessed on January 29, 2016