Adrenoleukodystrophy classification: Difference between revisions
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==Overview== | ==Overview== | ||
Adrenoleukodystrophy may be classified based on different clinical presentations. There are '''seven''' male phenotypes i.e. Childhood cerebral adrenoleukodystrophy, Adolescent, Adrenomyeloneuropathy, Adult cerebral, Olivo-pontocerebellar, Addison-only , Asymptomatic and '''five''' female phenotypes i.e. Asymptomatic, Mild myelopathy, Moderate to severe myeloneuropathy, Cerebral involvement, Clinically evident adrenal insufficiency. | |||
==Classification== | ==Classification== | ||
Latest revision as of 18:20, 10 June 2020
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Adrenoleukodystrophy Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Adrenoleukodystrophy classification On the Web |
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American Roentgen Ray Society Images of Adrenoleukodystrophy classification |
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Risk calculators and risk factors for Adrenoleukodystrophy classification |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
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Overview
Adrenoleukodystrophy may be classified based on different clinical presentations. There are seven male phenotypes i.e. Childhood cerebral adrenoleukodystrophy, Adolescent, Adrenomyeloneuropathy, Adult cerebral, Olivo-pontocerebellar, Addison-only , Asymptomatic and five female phenotypes i.e. Asymptomatic, Mild myelopathy, Moderate to severe myeloneuropathy, Cerebral involvement, Clinically evident adrenal insufficiency.
Classification
Adrenoleukodystrophy may be classified based on different clinical presentations. There are seven phenotypes described in males and five in females.[1]
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| Phenotype in Females |
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References
- ↑ Moser, Hugo W; Mahmood, Asif; Raymond, Gerald V (2007). "X-linked adrenoleukodystrophy". Nature Clinical Practice Neurology. 3 (3): 140–151. doi:10.1038/ncpneuro0421. ISSN 1745-834X.