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Assault by hunting rifle
Early-onset cerebellar ataxia with essential tremor
Hunt's ataxia
Myoclonus
Retained tendon reflexes
SCAR2

Translation of "hunt's ataxia " (English → French) :

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]
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]
https://icd.who.int/browse10/2 (...) [HTML]
Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo
https://browser.ihtsdotools.or (...) (...) [HTML]
ataxie spinocérébelleuse type 38
SNOMEDCT-BE (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo / 734021001
SNOMEDCT-BE (disorder) / 734021001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
A rare hereditary ataxia with characteristics of progressive cerebellar ataxia associated with disruption of visual fixation by saccadic intrusions. It presents with progressive gait, trunk and limb ataxia with pyramidal tract signs (increased tendon
https://browser.ihtsdotools.or (...) (...) [HTML]
syndrome d'ataxie cérébelleuse autosomique récessive-saccade oculaire
SNOMEDCT-BE (increased tendon / 766814006
SNOMEDCT-BE (disorder) / 766814006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
A very rare subtype of autosomal dominant cerebellar ataxia type 3 with characteristics of late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on
https://browser.ihtsdotools.or (...) (...) [HTML]
ataxie spinocérébelleuse type 26
SNOMEDCT-BE (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on / 718769009
SNOMEDCT-BE (disorder) / 718769009
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
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]
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]
https://browser.ihtsdotools.or (...) [HTML]
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]
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]
https://browser.ihtsdotools.or (...) [HTML]
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]
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]
https://browser.ihtsdotools.or (...) [HTML]
Assault by hunting rifle
https://browser.ihtsdotools.or (...) (...) [HTML]
agression avec un fusil de chasse
SNOMEDCT-BE (event) / 219204003
SNOMEDCT-BE (event) / 219204003
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
SCAR2 (spinocerebellar ataxia autosomal recessive 2)
https://browser.ihtsdotools.or (...) (...) [HTML]
ataxie cérébelleuse autosomique récessive type 3
SNOMEDCT-BE (spinocerebellar ataxia autosomal recessive 2) / 715369006
SNOMEDCT-BE (disorder) / 715369006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome
https://browser.ihtsdotools.or (...) (...) [HTML]
syndrome d'ataxie spastique-epilepsie myoclonique-neuropathie précoce
SNOMEDCT-BE (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome / 771469002
SNOMEDCT-BE (disorder) / 771469002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


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hunt's ataxia

Date index:2023-08-31 -

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