Olivopontocerebellar Atrophies

Synonyms

Ataxia, Presenile

Ataxias, Presenile

Atrophy, Familial Olivopontocerebellar

Atrophy, Idiopathic Olivopontocerebellar

Atrophy, Inherited Olivopontocerebellar

Atrophy, Nonfamilial Olivopontocerebellar

Atrophy, Olivo-Ponto-Cerebellar

Atrophy, Olivopontocerebellar

Atrophy, Pontoolivocerebellar

Degeneration, Olivo-Ponto-Cerebellar

Degeneration, Olivopontocerebellar

Degenerations, Olivo-Ponto-Cerebellar

Degenerations, Olivopontocerebellar

Dejerine Thomas Syndrome

Dejerine-Thomas Syndrome

Familial Olivopontocerebellar Atrophies

Familial Olivopontocerebellar Atrophy

Idiopathic Olivopontocerebellar Atrophies

Idiopathic Olivopontocerebellar Atrophy

Inherited Olivopontocerebellar Atrophies

Inherited Olivopontocerebellar Atrophy

Nonfamilial Olivopontocerebellar Atrophies

Nonfamilial Olivopontocerebellar Atrophy

Olivo Ponto Cerebellar Atrophy

Olivo Ponto Cerebellar Degeneration

Olivo-Ponto-Cerebellar Atrophy

Olivo-Ponto-Cerebellar Degeneration

Olivo-Ponto-Cerebellar Degenerations

Olivopontocerebellar Atrophies, Familial

Olivopontocerebellar Atrophies, Idiopathic

Olivopontocerebellar Atrophies, Inherited

Olivopontocerebellar Atrophies, Nonfamilial

Olivopontocerebellar Atrophy

Olivopontocerebellar Atrophy, Familial

Olivopontocerebellar Atrophy, Idiopathic

Olivopontocerebellar Atrophy, Inherited

Olivopontocerebellar Atrophy, Nonfamilial

Olivopontocerebellar Degeneration

Olivopontocerebellar Degenerations

Pontoolivocerebellar Atrophies

Pontoolivocerebellar Atrophy

Presenile Ataxia

Presenile Ataxias

Syndrome, Dejerine-Thomas

A group of inherited and sporadic disorders which share progressive ataxia in combination with atrophy of the CEREBELLUM; PONS; and inferior olivary nuclei. Additional clinical features may include MUSCLE RIGIDITY; NYSTAGMUS, PATHOLOGIC; RETINAL DEGENERATION; MUSCLE SPASTICITY; DEMENTIA; URINARY INCONTINENCE; and OPHTHALMOPLEGIA. The familial form has an earlier onset (second decade) and may feature spinal cord atrophy. The sporadic form tends to present in the fifth or sixth decade, and is considered a clinical subtype of MULTIPLE SYSTEM ATROPHY. (From Adams et al., Principles of Neurology, 6th ed, p1085)