A familial disorder associated with palatal myoclonus, other brainstem signs, tetraparesis, ataxia and Rosenthal fibre formation.

Three siblings presented with a progressive neurological disorder beginning in the third decade of life and characterised by palatal myoclonus, nystagmus, bulbar weakness and spastic tetraparesis. There was no evidence of intellectual deterioration or seizures. CT scan showed marked brainstem atroph...

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Detalhes bibliográficos

Publicado no:	J Neurol Neurosurg Psychiatry
Principais autores:	Howard, R S, Greenwood, R, Gawler, J, Scaravilli, F, Marsden, C D, Harding, A E
Formato:	Artigo
Idioma:	Inglês
Publicado em:	BMJ Publishing Group 1993
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC489732/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8410038/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jnnp.56.9.977
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