Adrenoleukodystrophy classification: Difference between revisions
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==Classification== | ==Classification== | ||
Adrenoleukodystrophy can be categorized based on different clinical presentations. There are '''seven''' phenotypes described in males and '''five''' in females. | Adrenoleukodystrophy can be categorized based on different clinical presentations. There are '''seven''' phenotypes described in males and '''five''' in females.<ref name="MoserMahmood2007">{{cite journal|last1=Moser|first1=Hugo W|last2=Mahmood|first2=Asif|last3=Raymond|first3=Gerald V|title=X-linked adrenoleukodystrophy|journal=Nature Clinical Practice Neurology|volume=3|issue=3|year=2007|pages=140–151|issn=1745-834X|doi=10.1038/ncpneuro0421}}</ref> | ||
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Revision as of 18:00, 10 June 2020
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Adrenoleukodystrophy Microchapters |
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Adrenoleukodystrophy classification On the Web |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
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Overview
Classification
Adrenoleukodystrophy can be categorized 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.