Cytochrome P450-oxidoreductase (POR) deficiency (ORD): Difference between revisions
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Created page with "__NOTOC__ {{SI}} {{CMG}}; {{AE}} {{MJ}} {{SK}} ==Overview== ==Historical Perspective== Congenital..." |
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==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
== Diagnosis == | == Diagnosis == | ||
Revision as of 19:48, 10 August 2017
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mehrian Jafarizade, M.D [2]
Synonyms and keywords:
Overview
Historical Perspective
Congenital adrenal hyperplasia was first discovered by Luigi De Crecchio, an Italian pathologist in 1865.[1]
Classification
There is no established classification system for lipoid congenital adrenal hyperplasia.
Pathophysiology
Causes
Differentiating [disease name] from other Diseases
Epidemiology and Demographics
Diagnosis
Symptoms
- Symptoms of [disease name] may include the following:
Physical Examination
- Physical examination may be remarkable for:
Laboratory Findings
Imaging Findings
Treatment
Medical Therapy
Surgery
References
- ↑ Delle Piane L, Rinaudo PF, Miller WL (2015). "150 years of congenital adrenal hyperplasia: translation and commentary of De Crecchio's classic paper from 1865". Endocrinology. 156 (4): 1210–7. doi:10.1210/en.2014-1879. PMID 25635623.