Spinocerebellar Degenerations [spinocerebelární degenerace]
- Terms
-
cerebelární ataxie s pozdním nástupem
cerebelární ataxie s raným nástupem
cerebelární ataxie, pozdní nástup
cerebelární ataxie, raný nástup
dědičné ataxie
dědičné spinocerebelární degenerace
kortikostriatálně-spinální degenerace
Marieova cerebelární ataxie
Marieova hereditární ataxie
Marinesco Sjogren syndrom
Marinesco-Sjogren syndrom
primární cerebelární degenerace
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Ataxias, Hereditary
Cerebellar Ataxia, Early Onset
Cerebellar Ataxia, Late Onset
Cerebellar Degenerations, Primary
Corticostriatal-Spinal Degeneration
Early Onset Cerebellar Ataxia
Familial Spinocerebellar Degenerations
Garland-Moorhouse Syndrome
Hereditary Oligophrenic Cerebello-Lental Degeneration
Hereditary Spinocerebellar Degenerations
Inherited Spinocerebellar Degenerations
Late Onset Cerebellar Ataxia
Marie Cerebellar Ataxia
Marie's Cerebellar Ataxia
Marinesco-Garland Syndrome
Marinesco-Sjogren Syndrome
Marinesco-Sjögren Syndrome
Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism
Marinesco-Sjogren Syndrome-Myopathy
Marinesco-Sjogren-Garland Syndrome
Spino Cerebellar Degenerations
Spino-Cerebellar Degenerations
Spinocerebellar Degeneration
Spinocerebellar Diseases
A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked.
- DUI
- D013132 MeSH Browser
- CUI
- M0020336
- Previous indexing
- Cerebellar Ataxia (1968-1986); Cerebellar Diseases (1966-1986); Spinal Cord Diseases (1966-1986)
- History note
- 2000(1987)
- Public note
- 2000; see SPINOCEREBELLAR DEGENERATION 1989-1999, see SPINOCEREBELLAR DEGENERATIONS 1987-1988
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 2
- CO
- complications 1
- CN
- congenital
- DI
- diagnosis 7
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy 1
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 2
- EH
- ethnology
- ET
- etiology 1
- GE
- genetics 6
- HI
- history 1
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 3
- PP
- physiopathology 7
- PC
- prevention & control
- PX
- psychology 1
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 3
- UR
- urine
- VE
- veterinary
- VI
- virology
Corneal cerebellar syndrome Disease MeSH Browser
Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy Disease MeSH Browser
Infantile onset spinocerebellar ataxia Disease MeSH Browser
Mousa Al din Al Nassar syndrome Disease MeSH Browser
Posterior column ataxia Disease MeSH Browser
Sensorimotor neuropathy with ataxia, autosomal dominant Disease MeSH Browser
Spinocerebellar Ataxia 29 Disease MeSH Browser
Spinocerebellar Ataxia, Autosomal Recessive 2 Disease MeSH Browser
Spinocerebellar ataxia 19 Disease MeSH Browser
Spinocerebellar ataxia 21 Disease MeSH Browser
Spinocerebellar ataxia 22 Disease MeSH Browser
Spinocerebellar ataxia 23 Disease MeSH Browser
Spinocerebellar ataxia 27 Disease MeSH Browser
Spinocerebellar ataxia 8 Disease MeSH Browser
Spinocerebellar ataxia, X-linked, 2 Disease MeSH Browser
Spinocerebellar ataxia, X-linked, 4 Disease MeSH Browser
Spinocerebellar ataxia, autosomal recessive 3 Disease MeSH Browser
Spinocerebellar ataxia, autosomal recessive 4 Disease MeSH Browser
Spinocerebellar ataxia, autosomal recessive 5 Disease MeSH Browser
Spinocerebellar ataxia, autosomal recessive 6 Disease MeSH Browser
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy Disease MeSH Browser