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Traduction de «Cerebellar congenital atrophy » (Anglais → Français) :

cerebellar congenital atrophy

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

atrophie cérébelleuse congénitale

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Aplasia of thyroid (with myxoedema) Congenital:atrophy of thyroid | hypothyroidism NOS

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

Aplasie de la thyroïde (avec myxœdème) Atrophie congénitale de la thyroïde Hypothyroïdie congénitale SAI

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

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hérédo-ataxie cérébelleuse

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olivo-ponto-cerebellar atrophy

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atrophie olivo-ponto-cérébelleuse

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atrophy of kidney:congenital | infantile | congenital absence of kidney

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absence congénitale de rein(s) atrophie rénale:congénitale | infantile

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Depressions in skull Deviation of nasal septum, congenital Hemifacial atrophy or hypertrophy Squashed or bent nose, congenital

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Atrophie ou hypertrophie hémifaciale Dépressions des os du crâne Déviation congénitale de la cloison nasale Ecrasement ou déviation congénital(e) du nez

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

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

A rare genetic neurological disorder characterized by late childhood onset of slowly progressive cerebellar ataxia. Initial manifestations include weakness and atrophy of distal limb muscles, areflexia and loss of pain, vibration and touch sensations

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syndrome d'ataxie spinocérébelleuse-neuropathie axonale type 1

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A genetic neurodegenerative disease with normal early development followed by childhood onset optic atrophy with progressive vision loss and eventually blindness, followed by progressive neurological decline that typically includes cerebellar ataxia,

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syndrome de neurodégénérescence progressive de l'enfant-cécité-ataxie-spasticité

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A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterized by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with

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syndrome d'ophtalmoplégie externe progressive-myopathie-émaciation

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D'autres ont cherché : marie disease marie's cerebellar ataxia marie's disease nonne-marie sydrome atrophy of kidney congenital cerebellar congenital atrophy congenital absence of kidney congenital cerebellar ataxia hypothyroidism nos infantile Cerebellar congenital atrophy

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'Cerebellar congenital atrophy' ->

Date index: 2022-03-20