| Descriptor English: | Olivopontocerebellar Atrophies | ||||||
| Descriptor Spanish: |
Atrofias Olivopontocerebelosas
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| Descriptor Portuguese: | Atrofias Olivopontocerebelares | ||||||
| Descriptor French: | Atrophies olivo-ponto-cérébelleuses | ||||||
| Entry term(s): |
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 Hypoplasia, Olivopontocerebellar 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 Olivopontocerebellar Hypoplasia Olivopontocerebellar Hypoplasias Pontoolivocerebellar Atrophies Pontoolivocerebellar Atrophy Presenile Ataxia Presenile Ataxias Syndrome, Dejerine-Thomas |
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| Tree number(s): |
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 C16.320.400.780.750 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D009849 | ||||||
| Scope note: | 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) |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Atrophy (1966-1986) Brain Diseases (1966-1986) Cerebellar Ataxia (1968-1986) Cerebellar Diseases (1966-1986) Olivary Nucleus (1966-1986) Pons (1966-1986) |
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| Public MeSH Note: | 2000; see OLIVOPONTOCEREBELLAR ATROPHY 1991-1999, see SPINOCEREBELLAR DEGENERATION 1987-1990 |
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| History Note: | 2000(1987) |
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| Entry Version: | OPCA |
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| Related: |
Multiple System Atrophy
MeSH | ||||||
| DeCS ID: | 19275 | ||||||
| Unique ID: | D009849 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1986/03/31 | ||||||
| Revision Date: | 2023/02/26 |
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Olivopontocerebellar Atrophies
- Preferred
Olivopontocerebellar Atrophy, Idiopathic
- Narrower
Familial Olivopontocerebellar Atrophy
- Narrower
Nonfamilial Olivopontocerebellar Atrophy
- Narrower
Olivopontocerebellar Hypoplasia
- Related but not broader or narrower
| Concept UI |
M0015287 |
| Scope note | 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) |
| Preferred term | Olivopontocerebellar Atrophies |
| Entry term(s) |
Ataxia, Presenile Ataxias, Presenile 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 Olivo Ponto Cerebellar Atrophy Olivo Ponto Cerebellar Degeneration Olivo-Ponto-Cerebellar Atrophy Olivo-Ponto-Cerebellar Degeneration Olivo-Ponto-Cerebellar Degenerations Olivopontocerebellar Atrophy Olivopontocerebellar Degeneration Olivopontocerebellar Degenerations Pontoolivocerebellar Atrophies Pontoolivocerebellar Atrophy Presenile Ataxia Presenile Ataxias Syndrome, Dejerine-Thomas |
| Concept UI |
M0332843 |
| Preferred term | Olivopontocerebellar Atrophy, Idiopathic |
| Entry term(s) |
Atrophy, Idiopathic Olivopontocerebellar Idiopathic Olivopontocerebellar Atrophies Idiopathic Olivopontocerebellar Atrophy Olivopontocerebellar Atrophies, Idiopathic |
| Concept UI |
M0332844 |
| Preferred term | Familial Olivopontocerebellar Atrophy |
| Entry term(s) |
Atrophy, Familial Olivopontocerebellar Atrophy, Inherited Olivopontocerebellar Familial Olivopontocerebellar Atrophies Inherited Olivopontocerebellar Atrophies Inherited Olivopontocerebellar Atrophy Olivopontocerebellar Atrophies, Familial Olivopontocerebellar Atrophies, Inherited Olivopontocerebellar Atrophy, Familial Olivopontocerebellar Atrophy, Inherited |
| Concept UI |
M0332845 |
| Preferred term | Nonfamilial Olivopontocerebellar Atrophy |
| Entry term(s) |
Atrophy, Nonfamilial Olivopontocerebellar Nonfamilial Olivopontocerebellar Atrophies Olivopontocerebellar Atrophies, Nonfamilial Olivopontocerebellar Atrophy, Nonfamilial |
| Concept UI |
M000758812 |
| Preferred term | Olivopontocerebellar Hypoplasia |
| Entry term(s) |
Hypoplasia, Olivopontocerebellar Olivopontocerebellar Hypoplasias |
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