Literature DB >> 6537856

Familial syndrome of deafness, myoclonus, and cerebellar ataxia.

S Chayasirisobhon, B Walters.   

Abstract

We report a case of identical twins with progressive sensorineural hearing loss, myoclonus, intention tremor, and ataxia. The involved member of the family may suggest of autosomal dominant transmission with variable penetrance.

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Mesh：

Year:  1984        PMID： 6537856     DOI： 10.1212/wnl.34.1.78

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


  2 in total

1.  SPECT, MRI and cognitive functions in multiple sclerosis.

Authors:  C Pozzilli; D Passafiume; S Bernardi; P Pantano; C Incoccia; S Bastianello; L Bozzao; G L Lenzi; C Fieschi
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-02       Impact factor: 10.154

2.  Abnormal muscle and skin mitochondria in family with myoclonus, ataxia, and deafness (May and White syndrome).

Authors:  J Vaamonde; J Muruzabal; T Tuñón; N Perez; J Artieda; M Rodriguez; J A Obeso
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-02       Impact factor: 10.154
  2 in total

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