Rare variability in adrenoleukodystrophy: a case report

BACKGROUND: X-linked adrenoleukodystrophy is a genetic disorder with diverse clinical phenotypes. Of these phenotypes, the cerebral form usually manifests during early childhood with rapid cognitive and neurological deterioration and is accompanied by extensive white matter involvement. Adrenomyelon...

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Detalles Bibliográficos
Autores principales: Chen, Yanming, Polara, Farhana, Pillai, Anjana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022434/
https://www.ncbi.nlm.nih.gov/pubmed/29950168
http://dx.doi.org/10.1186/s13256-018-1722-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6022434/
https://www.ncbi.nlm.nih.gov/pubmed/29950168
http://dx.doi.org/10.1186/s13256-018-1722-z

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