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

Friedreich ataxia

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

ataxia hereditaria | ataxie van Friedreich | spinale heredoataxia | tabes van Friedreich | ziekte van Friedreich

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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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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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Friedreich-like ataxia

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ataxie met vitamine E-deficiëntie

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

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cerebellaire heredo-ataxie

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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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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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ataxia | lack of coordination

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ataxie | onzekere gang

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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

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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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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.

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

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

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Date index: 2022-04-01