Syndrome is characterised by the combination of sensorineural hearing loss, early greying of scalp hair and adult onset essential tremor. It has been described in three unrelated individuals. Additional family members in each family showed varied exp

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syndrome de surdité neurosensorielle-grisonnement précoce-tremblement essentiel

SNOMEDCT-BE (disorder) / 723721007

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Early-onset cerebellar ataxia with:essential tremor | myoclonus [Hunt's ataxia] | retained tendon reflexes | Friedreich's ataxia (autosomal recessive) X-linked recessive spinocerebellar ataxia

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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

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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,

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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

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intention tremor | shakiness

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tremblement intentionnel | tremblement apparaissant au cours d'un mouvement volontaire (tremblement-)

UGENT - Medical terms -

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tremor

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trémor | tremblement