21-hydroxylase deficiency risk factors: Difference between revisions
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{{CMG}} {{AE}} {{AAM}} | {{CMG}} {{AE}} {{AAM}} | ||
==Overview== | ==Overview== | ||
The most potent risk factor in the development of congenital adrenal hyperplasia due to 21-hydroxylase deficiency is presence of [[family history]]. | |||
==Risk Factors== | ==Risk Factors== | ||
Presence of [[family history]] of congenital adrenal hyperplasia due to 21-hydroxylase deficiency is one of the most potent risk factors in disease development. | Presence of [[family history]] of congenital adrenal hyperplasia due to 21-hydroxylase deficiency is one of the most potent risk factors in disease development. | ||
Revision as of 14:36, 5 October 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 congenital adrenal hyperplasia due to 21-hydroxylase deficiency is presence of family history.
Risk Factors
Presence of family history of congenital adrenal hyperplasia due to 21-hydroxylase deficiency is one of the most potent risk factors in disease development.