Adrenoleukodystrophy classification

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Please help WikiDoc by adding content here. It’s easy! Click here to learn about editing.

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]


Phenotype in Females
Phenotype in Males
Childhood Cerebral Adrenoleukodystrophy (CCER)
Adolescent
Adrenomyeloneuropathy (AMN)
Adult cerebral
Olivo-pontocerebellar
Addison-only
Asymptomatic
Asymptomatic
Mild myelopathy
Moderate to severe myeloneuropathy
Cerebral involvement
Clinically evident adrenal insufficiency

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.

Template:WH Template:WS

[MoserMahmood2007-1] 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.

[1]

Adrenoleukodystrophy classification

Overview

Classification

References

Looking for the patient version?