Literature DB >> 1148822

Vestibular dysfunction in hereditary ataxia.

D V Philcox, S L Sellars, R Pamplett, P Beighton.   

Abstract

A kindred with a unique autosomal dominantly inherited ataxia of late onset is described. Manifestations of the condition include defective optokinetic nystagmus and absent or abnormal oculo-vestibular responses, in association with normal cochlear function. It is possible that these latter features may serve as "markers" to indicate the presence of the disease in presymptomatic young adults, thereby facilitating important genetic counseling.

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Year:  1975        PMID: 1148822     DOI: 10.1093/brain/98.2.309

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  2 in total

1.  Cellular hypersensitivity to brain antigen in children of a family with hereditary ataxia.

Authors:  R S Walls; D V Philcox; C L Cullis
Journal:  J Neurol Neurosurg Psychiatry       Date:  1979-03       Impact factor: 10.154

2.  Choline in hereditary ataxia.

Authors:  D V Philcox; B Kies
Journal:  Br Med J       Date:  1979-09-08
  2 in total

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