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Ataxia telangiectasia
Broken veins
Congenital cerebellar ataxia
Early-onset cerebellar ataxia with essential tremor
Familiar ataxia
Friedreich's spinal ataxia
Hereditary haemorrhagic telangiectasia
Hereditary spinal ataxia 2.Friedreich's disease
Hunt's ataxia
Louis-Bar
Marie ataxia
Marie disease
Marie's ataxia
Marie's cerebellar ataxia
Marie's disease
Myoclonus
Nonne-Marie sydrome
Retained tendon reflexes
Telangiectasia

Traduction de «Ataxia telangiectasia » (Anglais → Néerlandais) :

Ataxia telangiectasia [Louis-Bar]

ataxia teleangiectasia [Louis-Bar]


familiar ataxia | Friedreich's spinal ataxia | hereditary spinal ataxia 2.Friedreich's disease

ataxia hereditaria | ataxie van Friedreich | spinale heredo-ataxie van Friedreich | tabes van Friedreich


Marie ataxia | Marie's ataxia | Marie's cerebellar ataxia

cerebellaire heredo-ataxie


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

Friedreich-ataxie (autosomaal recessief) | vroeg optredende cerebellaire ataxie met | behouden peesreflexen | vroeg optredende cerebellaire ataxie met | essentiële tremor | vroeg optredende cerebellaire ataxie met | myoclonus [Hunts ataxie] | recessieve spinocerebellaire ataxie, X-gebonden


congenital cerebellar ataxia | Marie disease | Marie's cerebellar ataxia | Marie's disease | Nonne-Marie sydrome

erfelijke cerebellaire ataxie


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

spinocerebellaire ataxie type 38


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

autosomaal recessieve cerebellaire ataxie, korte oogbeweging-intrusie


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

spinocerebellaire ataxie type 26


telangiectasia | broken veins

teleangiëctasie | verwijding van de bloedvaten


Hereditary haemorrhagic telangiectasia

hereditaire hemorragische teleangiëctasie




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'Ataxia telangiectasia' ->

Date index: 2023-02-24
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