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Vertaling van "Marie's ataxia " (Engels → Nederlands) :

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

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cerebellaire heredo-ataxie

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Marie cerebellar ataxia

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hereditaire cerebellaire ataxie van Pierre Marie

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

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erfelijke cerebellaire ataxie

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

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

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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

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spinocerebellaire ataxie type 38

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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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Charcot-Marie-Tooth disease, type 4B2 (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso

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ziekte van Charcot-Marie-Tooth type 4B2

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Marie-Bamberger disease Pachydermoperiostosis

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pachydermoperiostose | ziekte van Marie-Bamberger

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Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome

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Anderen hebben gezocht naar : déjerine-sottas friedreich's spinal ataxia hunt's ataxia marie ataxia marie cerebellar ataxia marie disease marie's ataxia marie's cerebellar ataxia marie's disease nonne-marie sydrome congenital cerebellar ataxia familiar ataxia myoclonus retained tendon reflexes Marie's ataxia

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Marie's ataxia ->

Date index: 2021-02-14