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Disease Olivopontocerebellar Atrophies

Name Olivopontocerebellar Atrophies
Synonyms Ataxia, Presenile | Ataxias, Presenile | Atrophy, Familial Olivopontocerebellar | Atrophy, Idiopathic Olivopontocerebellar | Atrophy, Inherited Olivopontocerebellar | Atrophy, Nonfamilial Olivopontocerebellar | Atrophy, Olivopontocerebellar | Atrophy, Olivo-Ponto-Cerebellar | Atrophy, Pontoolivocerebellar | Degeneration, Olivopontocerebellar | Degeneration, Olivo-Ponto-Cerebellar | Degenerations, Olivopontocerebellar | Degenerations, Olivo-Ponto-Cerebellar | 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 | Olivopontocerebellar Atrophies, Familial | Olivopontocerebellar Atrophies, Idiopathic | Olivopontocerebellar Atrophies, Inherited | Olivopontocerebellar Atrophies, Nonfamilial | Olivopontocerebellar Atrophy | Olivo Ponto Cerebellar Atrophy | Olivo-Ponto-Cerebellar Atrophy | Olivopontocerebellar Atrophy, Familial | Olivopontocerebellar Atrophy, Idiopathic | Olivopontocerebellar Atrophy, Inherited | Olivopontocerebellar Atrophy, Nonfamilial | Olivopontocerebellar Degeneration | Olivo Ponto Cerebellar Degeneration | Olivo-Ponto-Cerebellar Degeneration | Olivopontocerebellar Degenerations | Olivo-Ponto-Cerebellar Degenerations | Pontoolivocerebellar Atrophies | Pontoolivocerebellar Atrophy | Presenile Ataxia | Presenile Ataxias | Syndrome, Dejerine-Thomas
Definition 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)
Categories Genetic disease (inborn) | Nervous system disease
MeSH® ID D009849
External Links

Top ↑ Ancestors

1. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Autonomic Nervous System Diseases Has associated chemicals Has associated genes Primary Dysautonomias Has associated chemicals Has associated genes Multiple System Atrophy Has associated chemicals Has associated genes Olivopontocerebellar Atrophies Has associated chemicals Has associated genes
2. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Central Nervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Brain Diseases Has associated chemicals Has associated genes Has associated exposure references Basal Ganglia Diseases Has associated chemicals Has associated genes Has associated exposure references Multiple System Atrophy Has associated chemicals Has associated genes Olivopontocerebellar Atrophies Has associated chemicals Has associated genes
3. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Central Nervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Brain Diseases Has associated chemicals Has associated genes Has associated exposure references Cerebellar Diseases Has associated chemicals Has associated genes Spinocerebellar Degenerations Has associated chemicals Has associated genes Olivopontocerebellar Atrophies Has associated chemicals Has associated genes
4. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Central Nervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Movement Disorders Has associated chemicals Has associated genes Has associated exposure references Multiple System Atrophy Has associated chemicals Has associated genes Olivopontocerebellar Atrophies Has associated chemicals Has associated genes
5. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Central Nervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Spinal Cord Diseases Has associated chemicals Has associated genes Has associated exposure references Spinocerebellar Degenerations Has associated chemicals Has associated genes Olivopontocerebellar Atrophies Has associated chemicals Has associated genes
6. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Neurodegenerative Diseases Has associated chemicals Has associated genes Has associated exposure references Heredodegenerative Disorders, Nervous System Has associated chemicals Has associated genes Spinocerebellar Degenerations Has associated chemicals Has associated genes Olivopontocerebellar Atrophies Has associated chemicals Has associated genes
7. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Neurodegenerative Diseases Has associated chemicals Has associated genes Has associated exposure references Multiple System Atrophy Has associated chemicals Has associated genes Olivopontocerebellar Atrophies Has associated chemicals Has associated genes
8. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Heredodegenerative Disorders, Nervous System Has associated chemicals Has associated genes Spinocerebellar Degenerations Has associated chemicals Has associated genes Olivopontocerebellar Atrophies Has associated chemicals Has associated genes

Top ↑ Descendants

Olivopontocerebellar Atrophies Has associated chemicals Has associated genes
  Microcephaly pontocerebellar hypoplasia dyskinesia
  Olivopontocerebellar atrophy 1
  Olivopontocerebellar atrophy 3
  Olivopontocerebellar Atrophy II, Autosomal Recessive
  Olivopontocerebellar Atrophy V
  Olivopontocerebellar hypoplasia, fetal-onset
  Pontocerebellar Hypoplasia Type 1 Has associated chemicals Has associated genes
  Pontocerebellar Hypoplasia Type 2
  Pontocerebellar Hypoplasia Type 2A Has associated chemicals Has associated genes
  Pontocerebellar Hypoplasia Type 3 Has associated chemicals Has associated genes
  Pontocerebellar Hypoplasia Type 6 Has associated chemicals Has associated genes
  Spinocerebellar Ataxia, X-Linked 1
  Spinocerebellar Atrophy With Pupillary Paralysis
View node Young McKeever Squier syndrome Has associated chemicals Has associated genes