Search on: OLIVOPONTOCEREBELLAR ATROPHIES 
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Descriptor English:   Olivopontocerebellar Atrophies 
Descriptor Spanish:   Atrofias Olivopontocerebelosas 
Descriptor Portuguese:   Atrofias Olivopontocerebelares 
Synonyms English:   Familial Olivopontocerebellar Atrophy
Inherited Olivopontocerebellar Atrophy
Nonfamilial Olivopontocerebellar Atrophy
Olivo-Ponto-Cerebellar Atrophy
Olivo-Ponto-Cerebellar Degeneration
Olivopontocerebellar Atrophy
Olivopontocerebellar Degeneration
Pontoolivocerebellar Atrophy
Presenile Ataxia
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
Familial Olivopontocerebellar Atrophies
Idiopathic Olivopontocerebellar Atrophies
Idiopathic Olivopontocerebellar Atrophy
Inherited Olivopontocerebellar Atrophies
Nonfamilial Olivopontocerebellar Atrophies
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, Familial
Olivopontocerebellar Atrophy, Inherited
Olivopontocerebellar Atrophy, Nonfamilial
Olivopontocerebellar Degenerations
Pontoolivocerebellar Atrophies
Presenile Ataxias
Syndrome, Dejerine-Thomas
Dejerine-Thomas Syndrome
Olivopontocerebellar Atrophy, Idiopathic  
Tree Number:   C10.177.575.550.375
C10.228.140.079.612.600
C10.228.140.252.700.650
C10.228.662.550.600
C10.228.854.787.750
C10.574.500.825.650
C10.574.625.600
C16.320.400.780.750
Definition English:   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) 
See Related English:   Multiple System Atrophy
 
History Note English:   2000(1987) 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications CN congenital
DI diagnosis DG diagnostic imaging
DH diet therapy DT drug therapy
EC economics EM embryology
EN enzymology EP epidemiology
EH ethnology ET etiology
GE genetics HI history
IM immunology ME metabolism
MI microbiology MO mortality
NU nursing PS parasitology
PA pathology PP physiopathology
PC prevention & control PX psychology
RT radiotherapy RH rehabilitation
SU surgery TH therapy
UR urine VE veterinary
VI virology  
Record Number:   19275 
Unique Identifier:   D009849 

Occurrence in VHL: 		 

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