Early onset hereditary spinocerebellar ataxia: an autosomal recessive disorder distinct from Friedreich's ataxia.

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dc.contributor.authorKumar, Den_US
dc.contributor.authorBlank, C Een_US
dc.date.accessioned1989-10-01en_US
dc.date.accessioned2009-05-27T05:58:55Z
dc.date.available1989-10-01en_US
dc.date.available2009-05-27T05:58:55Z
dc.date.issued1989-10-01en_US
dc.description.abstractThe important clinical features of seven patients with an early onset slowly progressive heredofamilial spinocerebellar degenerative disorder of probably autosomal recessive inheritance included limb ataxia, retained and/or exaggerated tendon reflexes (biceps and knee), pyramidal weakness of lower limbs and normal sensory action potentials. This rare disorder is probably distinct from Friedreich's ataxia and carries a better prognosis.en_US
dc.identifier.citationKumar D, Blank CE. Early onset hereditary spinocerebellar ataxia: an autosomal recessive disorder distinct from Friedreich's ataxia. Indian Pediatrics. 1989 Oct; 26(10): 1014-9en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/14270
dc.language.isoengen_US
dc.source.urihttps://indianpediatrics.neten_US
dc.subject.meshAdolescenten_US
dc.subject.meshAdulten_US
dc.subject.meshChilden_US
dc.subject.meshChild, Preschoolen_US
dc.subject.meshDiagnosis, Differentialen_US
dc.subject.meshFemaleen_US
dc.subject.meshFriedreich Ataxia --diagnosisen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshSpinocerebellar Degenerations --diagnosisen_US
dc.titleEarly onset hereditary spinocerebellar ataxia: an autosomal recessive disorder distinct from Friedreich's ataxia.en_US
dc.typeJournal Articleen_US
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