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Vertaling van "familiar ataxia " (Engels → Nederlands) :

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

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

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

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

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cerebellaire heredo-ataxie

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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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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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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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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

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spinocerebellaire ataxie type 26

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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

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autosomaal recessieve cerebellaire ataxie, korte oogbeweging-intrusie

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ataxia | lack of coordination

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ataxie | onzekere gang

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Definition: A condition, so far found only in girls, in which apparently normal early development is followed by partial or complete loss of speech and of skills in locomotion and use of hands, together with deceleration in head growth, usually with an onset between seven and 24 months of age. Loss of purposive hand movements, hand-wringing stereotypies, and hyperventilation are characteristic. Social and play development are arrested but social interest tends to be maintained. Trunk ataxia and apraxia start to develop by age four years and choreoathetoid movements frequently follow. Severe mental retardation almost invariably results.

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Omschrijving: Een toestand, tot dusver alleen bij meisjes aangetroffen, waarin een ogenschijnlijk normale vroege ontwikkeling wordt gevolgd door gedeeltelijk of volledig verlies van spraak en vaardigheid in voortbeweging en gebruik van handen, begeleid door afname van de schedelgroei, die doorgaans aan het licht treedt op de leeftijd van 7 tot 24 maanden. Verlies van doelgerichte handbewegingen, handenwringende stereotypieën en hyperventilatie zijn kenmerkend. Sociale ontwikkeling en ontwikkeling van het spelen komen tot stilstand, maar de sociale belangstelling blijft meestal intact. Rompataxie en -apraxie beginnen zich te ontwikkelen o ...[+++]

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Definition: In the commonest varieties there is loss of ability to move the whole or a part of a limb or limbs. There may be close resemblance to almost any variety of ataxia, apraxia, akinesia, aphonia, dysarthria, dyskinesia, seizures, or paralysis. | Psychogenic:aphonia | dysphonia

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Omschrijving: Bij de meest voorkomende vormen is er verlies van het vermogen een lidmaat of ledematen geheel of gedeeltelijk te bewegen. Er kan een sterke overeenkomst bestaan met bijna elke vorm van ataxie, apraxie, akinesie, afonie, dysartrie, dyskinesie, attaque of verlamming. | Neventerm: | psychogene afonie | psychogene dysfonie

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https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]

Anderen hebben gezocht naar : friedreich's spinal ataxia hunt's ataxia marie ataxia marie disease marie's ataxia marie's cerebellar ataxia marie's disease nonne-marie sydrome psychogenic aphonia ataxia congenital cerebellar ataxia dysphonia familiar ataxia lack of coordination myoclonus retained tendon reflexes

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Date index: 2021-02-09