Adult onset Krabbe disease may mimic motor neurone disease


Autoria(s): Henderson, R. D.; MacMillan, J. C.; Bradfield, J. M.
Contribuinte(s)

A. H. Kaye

S. Davis

Data(s)

01/09/2003

Resumo

Krabbe's disease (galactocerebrosidase deficiency) rarely presents in adults, usually with predominantly upper motor neurone clinical features. We report a case in whom the clinical features were similar to motor neurone disease. Nerve conduction studies and neuroimaging were important in leading to the correct diagnosis. Differences in adult-onset presentations are described. (C) 2003 Elsevier Science Ltd. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:64780

Idioma(s)

eng

Publicador

Churchill Livingstone

Palavras-Chave #Clinical neurology #Neurosciences #Krabbe disease #Motor neurone disease #Galactocerebrosidase #Globoid cell leukodystrophy #C1 #321013 Neurology and Neuromuscular Diseases #730104 Nervous system and disorders #1103 Clinical Sciences
Tipo

Journal Article