11β-hydroxylase deficiency risk factors: Difference between revisions
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==Overview== | ==Overview== | ||
The most potent risk factor in the development of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency is presence of [[family history]] of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. | |||
== | ==Risk Factors== | ||
The most potent risk factor in the development of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency is presence of [[family history]] of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. | |||
==References== | ==References== | ||
{{Relist|2}} | {{Relist|2}} |
Revision as of 18:46, 28 January 2016
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency Microchapters |
Differentiating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency from other Diseases |
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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
The most potent risk factor in the development of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency is presence of family history of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.
Risk Factors
The most potent risk factor in the development of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency is presence of family history of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.
References