Olivopontocerebellar Atrophies [olivopontocerebelární atrofie]
- 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
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
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications 1
- CN
- congenital
- DI
- diagnosis 3
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 5
- GE
- genetics 6
- HI
- history
- IM
- immunology 1
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 4
- PP
- physiopathology 9
- PC
- prevention & control
- PX
- psychology 1
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 1
- UR
- urine
- VE
- veterinary 2
- VI
- virology
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