11β-hydroxylase deficiency classification: Difference between revisions
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==Overview== | ==Overview== | ||
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency may be classified according to clinical presentation into 2 subtypes: classic form and the non-classic form. | |||
==Classification== | ==Classification== | ||
There are two types of | There are two types of Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency, the classic form and the non-classic form. The classic form is the more severe of the two types. | ||
==Reference== | ==Reference== | ||
{{Reflist|2}} | {{Reflist|2}} | ||
Revision as of 11:21, 28 January 2016
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Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency Microchapters |
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Differentiating Congenital adrenal hyperplasia due to 11β-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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11β-hydroxylase deficiency classification On the Web |
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American Roentgen Ray Society Images of 11β-hydroxylase deficiency classification |
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Directions to Hospitals Treating Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency |
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Risk calculators and risk factors for 11β-hydroxylase deficiency classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency may be classified according to clinical presentation into 2 subtypes: classic form and the non-classic form.
Classification
There are two types of Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency, the classic form and the non-classic form. The classic form is the more severe of the two types.