21-hydroxylase deficiency causes: Difference between revisions
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{{CMG}} {{AE}} {{AAM}} | {{CMG}} {{AE}} {{AAM}} | ||
==Overview== | ==Overview== | ||
Congenital adrenal hyperplasia is caused by mutations in the CYP21A2 gene, which cause 21-hydroxylase deficiency. | |||
==Causes== | ==Causes== | ||
Congenital adrenal hyperplasia is caused by mutations in the CYP21A2 gene, which cause 21-hydroxylase deficiency. | |||
== References == | == References == | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Revision as of 20:28, 14 September 2015
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Congenital adrenal hyperplasia due to 21-hydroxylase deficiency Microchapters |
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Differentiating Congenital adrenal hyperplasia due to 21-hydroxylase deficiency from other Diseases |
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Diagnosis |
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Treatment |
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Case Studies |
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21-hydroxylase deficiency causes On the Web |
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American Roentgen Ray Society Images of 21-hydroxylase deficiency causes |
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Directions to Hospitals Treating Congenital adrenal hyperplasia due to 21-hydroxylase deficiency |
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Risk calculators and risk factors for 21-hydroxylase deficiency causes |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]
Overview
Congenital adrenal hyperplasia is caused by mutations in the CYP21A2 gene, which cause 21-hydroxylase deficiency.
Causes
Congenital adrenal hyperplasia is caused by mutations in the CYP21A2 gene, which cause 21-hydroxylase deficiency.