Olivopontocerebellar Atrophies [olivopontocerebelární atrofie]

topical
21
Terms

familiární olivopontocerebelární atrofie
idiopatická olivopontocerebelární atrofie
nefamiliární olivopontocerebelární atrofie
olivopontocerebelární atrofie idiopatická
OPCA

 

Dejerine-Thomas Syndrome
Familial Olivopontocerebellar Atrophy
Inherited Olivopontocerebellar Atrophy
Nonfamilial Olivopontocerebellar Atrophy
Olivo-Ponto-Cerebellar Atrophy
Olivo-Ponto-Cerebellar Degeneration
Olivopontocerebellar Atrophy
Olivopontocerebellar Atrophy, Idiopathic
Olivopontocerebellar Degeneration
Olivopontocerebellar Hypoplasia
Pontoolivocerebellar Atrophy
Presenile Ataxia

Persistent link   https://www.medvik.cz/link/D009849
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)

DUI
D009849 MeSH Browser
CUI
M0015287
Previous indexing
Cerebellar Ataxia (1968-1986); Cerebellar Diseases (1966-1986); Atrophy (1966-1986); Brain Diseases (1966-1986); Olivary Nucleus (1966-1986); Pons (1966-1986)
History note
2000(1987)
Public note
2000; see OLIVOPONTOCEREBELLAR ATROPHY 1991-1999, see SPINOCEREBELLAR DEGENERATION 1987-1990

C Diseases
C10.177.575.550 Multiple System Atrophy 56
C10.177.575.550.375 Olivopontocerebellar Atrophies 21
C10.177.575.550.750 Shy-Drager Syndrome 5
C10.177.575.550.875 Striatonigral Degeneration 4
C10.228.140 Brain Diseases 1 178
C10.228.140.079 Basal Ganglia Diseases 100
C10.228.140.079.612 Multiple System Atrophy 56
C10.228.140.079.612.600 Olivopontocerebellar Atrophies 21
C10.228.140.079.612.700 Shy-Drager Syndrome 5
C10.228.140.079.612.800 Striatonigral Degeneration 4
C10.228.140.252 Cerebellar Diseases 165
C10.228.140.252.700 Spinocerebellar Degenerations 30
C10.228.140.252.700.150 Friedreich Ataxia 54
C10.228.140.252.700.250 Myoclonic Cerebellar Dyssynergia
C10.228.140.252.700.650 Olivopontocerebellar Atrophies 21
C10.228.140.252.700.700 Spinocerebellar Ataxias 74
C10.228.662 Movement Disorders 914
C10.228.662.550 Multiple System Atrophy 56
C10.228.662.550.600 Olivopontocerebellar Atrophies 21
C10.228.662.550.700 Shy-Drager Syndrome 5
C10.228.662.550.800 Striatonigral Degeneration 4
C10.228.854 Spinal Cord Diseases 310
C10.228.854.787.200 Friedreich Ataxia 54
C10.228.854.787.750 Olivopontocerebellar Atrophies 21
C10.228.854.787.875 Spinocerebellar Ataxias 74
C10.574.500.825.200 Friedreich Ataxia 54
C10.574.500.825.650 Olivopontocerebellar Atrophies 21
C10.574.500.825.700 Spinocerebellar Ataxias 74
C16.320.400.780.200 Friedreich Ataxia 54
C16.320.400.780.750 Olivopontocerebellar Atrophies 21
C16.320.400.780.875 Spinocerebellar Ataxias 74

Microcephaly pontocerebellar hypoplasia dyskinesia Disease MeSH Browser

Olivopontocerebellar Atrophy II, Autosomal Recessive Disease MeSH Browser

Olivopontocerebellar Atrophy V Disease MeSH Browser

Olivopontocerebellar atrophy 1 Disease MeSH Browser

Olivopontocerebellar atrophy 3 Disease MeSH Browser

Olivopontocerebellar hypoplasia, fetal-onset Disease MeSH Browser

Pontocerebellar Hypoplasia Type 1 Disease MeSH Browser

Pontocerebellar Hypoplasia Type 2 Disease MeSH Browser

Pontocerebellar Hypoplasia Type 2A Disease MeSH Browser

Pontocerebellar Hypoplasia Type 3 Disease MeSH Browser

Pontocerebellar Hypoplasia Type 6 Disease MeSH Browser

Spinocerebellar Ataxia, X-Linked 1 Disease MeSH Browser

Spinocerebellar Atrophy With Pupillary Paralysis Disease MeSH Browser