Literature DB >> 559257

Familial spastic ataxia: occurrence in childhood.

G W Hogan, M L Bauman.   

Abstract

The childhood form of familial spastic ataxia differs in many aspects from the disease of adult onset but as yet has received little attention in the literature. Five children with familial spastic ataxia are presented. A general review of the pertinent literature on familial spastic ataxia is included. The clinical and pathologic features of the childhood form of this disease are variable. Because this recessive disease has no known metabolic marker, differential diagnosis is difficult, requiring detailed history and careful observation.

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Year:  1977        PMID: 559257     DOI: 10.1212/wnl.27.6.520

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


  4 in total

1.  A syndrome of early onset spinocerebellar ataxia with optic atrophy, internuclear ophthalmoplegia, dementia, and startle myoclonus in a Sri Lankan family.

Authors:  N Senanayake
Journal:  J Neurol       Date:  1992-05       Impact factor: 4.849

2.  Early onset cerebellar ataxia with retained tendon reflexes: a clinical and genetic study of a disorder distinct from Friedreich's ataxia.

Authors:  A E Harding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1981-06       Impact factor: 10.154

3.  Spontaneous expression of the chromosome fragile site fra(10)(q25).

Authors:  A M Taylor; S Bundey
Journal:  Am J Hum Genet       Date:  1983-01       Impact factor: 11.025

4.  Optic nerve hypoplasia associated with pupillary light-near dissociation, spastic paraparesis and other non-ocular anomalies.

Authors:  D Doro; A Rossetti; P A Battistella; P Fardin; F Moro
Journal:  Ital J Neurol Sci       Date:  1988-10
  4 in total

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