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CPEO
CR3
Cell membrane receptor complex
Chronic chorea
Chronic progressive chorea
Chronic progressive external ophthalmoplegia
Chronic progressive hereditary chorea
Degenerative chorea
Dementia in Huntington's chorea
HD
Hereditary chorea
Huntington chorea
Huntington disease
Huntington's chorea
Huntington's disease

Traduction de «Chronic progressive chorea » (Anglais → Français) :

Huntington's chorea | chronic progressive hereditary chorea | chronic progressive chorea | degenerative chorea | hereditary chorea | Huntington's disease | HD

chorée de Huntington | chorée héréditaire | chorée chronique | maladie de Huntington


chronic progressive hereditary chorea | Huntington chorea | Huntington disease | Huntington's chorea | Huntington's disease | HD [Abbr.]

chorée de Huntington | chorée d'Huntington | chorée héréditaire | maladie de Huntington


chronic progressive external ophthalmoplegia | CPEO [Abbr.]

ophtalmoplégie externe progressive chronique


A rare genetic disorder of thiamine metabolism and transport with characteristics of the childhood-onset of recurrent episodes of flaccid paralysis and encephalopathy, associated with bilateral striatal necrosis and chronic progressive axonal polyneu

polyneuropathie progressive avec nécrose striatale bilatérale


degenerative chorea [ chronic chorea ]

chorée variable des dégénérés


A rare genetic neuromuscular disease with characteristics of acute episodic muscle weakness in upper and lower extremities (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy.

paralysie périodique avec neuropathie motrice distale tardive


A rare Huntington disease-like syndrome with characteristics of childhood-onset progressive neurologic deterioration with pyramidal and extrapyramidal abnormalities, chorea, dystonia, ataxia, gait instability, spasticity, seizures, mutism, and (on br

maladie de Huntington-like 3


Definition: A dementia occurring as part of a widespread degeneration of the brain. The disorder is transmitted by a single autosomal dominant gene. Symptoms typically emerge in the third and fourth decade. Progression is slow, leading to death usually within 10 to 15 years. | Dementia in Huntington's chorea

Définition: Démence survenant dans le contexte d'une dégénérescence cérébrale étendue. La maladie est transmise par un gène autosomique dominant unique. Les symptômes apparaissent typiquement dans la troisième et la quatrième décennies. L'évolution est lentement progressive, aboutissant habituellement à la mort en 10 à 15 années. | Démence de la chorée de Huntington


Definition: A chronic stage in the development of a schizophrenic illness in which there has been a clear progression from an early stage to a later stage characterized by long- term, though not necessarily irreversible, negative symptoms, e.g. psychomotor slowing; underactivity; blunting of affect; passivity and lack of initiative; poverty of quantity or content of speech; poor nonverbal communication by facial expression, eye contact, voice modulation and posture; poor self-care and social performance. | Chronic undifferentiat ...[+++]

Définition: Stade chronique de l'évolution d'une maladie schizophrénique, avec une progression nette à partir du début jusqu'à un stade tardif caractérisé par des symptômes négatifs durables, mais pas obligatoirement irréversibles, par exemple ralentissement psychomoteur, hypoactivité, émoussement affectif, passivité et manque d'initiative, pauvreté de la quantité et du contenu du discours, peu de communication non verbale (expression faciale, contact oculaire, modulation de la voix et gestes), manque de soins apportés à sa personne e ...[+++]


Cell membrane receptor complex [CR3] defect Chronic (childhood) granulomatous disease Congenital dysphagocytosis Progressive septic granulomatosis

Déficit en complexe récepteur de la membrane cellulaire [CR3] Dysphagocytose congénitale Granulomatose septique progressive Maladie granulomateuse chronique (infantile)




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Date index: 2022-03-19
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