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Early-onset cerebellar ataxia with essential tremor
Hunt's ataxia
Myoclonus
Retained tendon reflexes
SCA1
SCA2
Spinocerebellar ataxia
Spinocerebellar ataxia 1
Spinocerebellar ataxia 2
Spinocerebellar ataxia II
Spinocerebellar ataxia type 1
Spinocerebellar ataxia type 2
Type 1 spinocerebellar ataxia

Translation of "Spinocerebellar ataxia type 2 " (English → French) :

Spinocerebellar ataxia type 28 (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
ataxie spinocérébelleuse type 28
SNOMEDCT-BE (SCA28) is very rare with main features of juvenile onset and slowly progressive cerebellar ataxia due to Purkinje cell degeneration. The mean age of symptom onset was 19.5 years in the original kindred. Some patients s / 715824008
SNOMEDCT-BE (disorder) / 715824008
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Spinocerebellar ataxia type 29 (SCA29) is a rare disease with main features of very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability. SCA29 presents at birth, or shortly, after with manife
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
ataxie spinocérébelleuse type 29
SNOMEDCT-BE (SCA29) is a rare disease with main features of very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability. SCA29 presents at birth, or shortly, after with manife / 715825009
SNOMEDCT-BE (disorder) / 715825009
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
spinocerebellar ataxia 1 | SCA1 | type 1 spinocerebellar ataxia | spinocerebellar ataxia type 1
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
ataxie spinocérébelleuse 1 | ataxie spinocérébellaire 1 | ataxie spino-cérébelleuse de type I | ataxie spinocérébelleuse de type 1 | SCA 1
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
spinocerebellar ataxia 2 | SCA2 | spinocerebellar ataxia type 2 | spinocerebellar ataxia II
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
ataxie spinocérébelleuse 2 | SCA2
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
Spinocerebellar ataxia type 31 (SCA31) is a very rare disease with manifestation of late-onset of cerebral ataxia, dysarthria, and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense,
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
ataxie spinocérébelleuse type 31
SNOMEDCT-BE (SCA31) is a very rare disease with manifestation of late-onset of cerebral ataxia, dysarthria, and horizontal gaze nystagmus, and that is occasionally accompanied by pyramidal signs, tremor, decreased vibration sense, / 715826005
SNOMEDCT-BE (disorder) / 715826005
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Early-onset cerebellar ataxia with:essential tremor | myoclonus [Hunt's ataxia] | retained tendon reflexes | Friedreich's ataxia (autosomal recessive) X-linked recessive spinocerebellar ataxia
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Ataxie (de):cérébelleuse précoce avec:myoclonies [Ramsay-Hunt] | persistance des réflexes tendineux | tremblement essentiel | Friedreich (autosomique récessive) | spino-cérébelleuse récessive liée au chromosome X
WORLD HEALTH ORGANIZATION ICD-10: G11.1
WORLD HEALTH ORGANIZATION ICD-10: G11.1
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
spinocerebellar ataxia
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
ataxie spinocérébelleuse
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]


Others have searched : hunt's ataxia    myoclonus    retained tendon reflexes    spinocerebellar ataxia    spinocerebellar ataxia ii    spinocerebellar ataxia type    type 1 spinocerebellar ataxia    Spinocerebellar ataxia type 2    


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'Spinocerebellar ataxia type 2'

Date index:2022-08-24 -

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