21-hydroxylase deficiency risk factors: Difference between revisions
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==Overview== | ==Overview== | ||
The most potent risk factor in the development of 21-hydroxylase deficient [[congenital adrenal hyperplasia]] is [[ | The most potent risk factor in the development of 21-hydroxylase deficient [[congenital adrenal hyperplasia]] is [[mutation]]s in the ''CYP21A2'' gene. | ||
==Risk Factors== | ==Risk Factors== | ||
[[Mutation]]s in the ''CYP21A2'' gene cause 21-hydroxylase deficient congenital adrenal hyperplasia. | [[Mutation]]s in the ''CYP21A2'' gene cause 21-hydroxylase deficient congenital adrenal hyperplasia. | ||
Revision as of 13:52, 16 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 risk factors On the Web |
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American Roentgen Ray Society Images of 21-hydroxylase deficiency risk factors |
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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 risk factors |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Ahmad Al Maradni, M.D. [2]
Overview
The most potent risk factor in the development of 21-hydroxylase deficient congenital adrenal hyperplasia is mutations in the CYP21A2 gene.
Risk Factors
Mutations in the CYP21A2 gene cause 21-hydroxylase deficient congenital adrenal hyperplasia.