Clinical features and molecular genetics of autosomal recessive cerebellar ataxias.

Abstract excerpt

Among the hereditary ataxias, autosomal recessive spinocerebellar ataxias comprise a diverse group of neurodegenerative disorders. Clinical phenotypes vary from predominantly cerebellar syndromes to sensorimotor neuropathy, ophthalmological disturbances, involuntary movements, seizures, cognitive dysfunction, skeletal anomalies, and cutaneous disorders, among others. Molecular pathogenesis also ranges from...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Atrophy
• Share to Cerebellar Ataxia
• Share to Cerebellum