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Hemiplegia
Paralysis of one side
Spastic hemiplegia

Translation of "spastic hemiplegia " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Spastic hemiplegia

hémiplégie spastique
SNOMEDCT-BE (disorder) / 79633009
SNOMEDCT-BE (disorder) / 79633009


Spastic hemiplegia

Hémiplégie spastique
WORLD HEALTH ORGANIZATION ICD-10: G81.1
WORLD HEALTH ORGANIZATION ICD-10: G81.1


hemiplegia | paralysis of one side

hémiplégie | hémiplégie
UGENT - Medical terms -
UGENT - Medical terms -


AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome

syndrome d'ataxie spastique-epilepsie myoclonique-neuropathie précoce
SNOMEDCT-BE (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome / 771469002
SNOMEDCT-BE (disorder) / 771469002


Syndrome with characteristics of precocious puberty (due to Leydig cell hyperplasia), progressive spastic paraplegia and intellectual deficit. It has been described in two brothers. The fact that other family members displayed brisk reflexes and dysa

syndrome de parésie spastique-puberté précoce
SNOMEDCT-BE (due to Leydig cell hyperplasia), progressive spastic paraplegia and intellectual deficit. It has been described in two brothers. The fact that other family members displayed brisk reflexes and dysa / 732958004
SNOMEDCT-BE (disorder) / 732958004


A rare complex spastic paraplegia with characteristics of early onset hypotonia that progresses to spasticity, global developmental delay, severe intellectual disability and speech impairment, microcephaly, short stature and dysmorphic features. Pati

déficience intellectuelle sévère et paraplégie spastique progressive
SNOMEDCT-BE (disorder) / 778011005
SNOMEDCT-BE (disorder) / 778011005


A form of hereditary spastic paraplegia with onset usually in adulthood of progressive bilateral lower limb weakness and spasticity, sphincter dysfunction, decreased vibratory sense at the ankles and with additional manifestations including optical n

paraplégie spastique type 7
SNOMEDCT-BE (disorder) / 715776003
SNOMEDCT-BE (disorder) / 715776003


Congenital spastic paralysis (cerebral) Spastic cerebral palsy NOS

Paralysie cérébrale spastique SAI
WORLD HEALTH ORGANIZATION ICD-10: G80.1
WORLD HEALTH ORGANIZATION ICD-10: G80.1


A rare mitochondrial substrate carrier disorder with characteristics of severe muscular hypotonia, seizures beginning in the first year of life and arrested psychomotor development (affecting mainly motor skills). Severe spasticity with hyperreflexia

encéphalopathie épileptique avec démyélinisation cérébrale généralisée
SNOMEDCT-BE (affecting mainly motor skills). Severe spasticity with hyperreflexia / 726702005
SNOMEDCT-BE (disorder) / 726702005


A rare genetic neurodegenerative disorder characterized by progressive psychomotor and cognitive regression (manifesting with gait ataxia, spasticity, loss of language, mild to severe intellectual disability, pyramidal and extrapyramidal signs and, f

syndrome neurodégénératif sévère avec lipodystrophie
SNOMEDCT-BE (manifesting with gait ataxia, spasticity, loss of language, mild to severe intellectual disability, pyramidal and extrapyramidal signs and, f / 773555005
SNOMEDCT-BE (disorder) / 773555005
IN-CONTEXT TRANSLATIONS
The incidence and the severity of malnutrition in NI children increases with the duration and the severity of neurological impairment [7][11][12]. Growth of children with spastic quadriplegia is more severely affected, but children with diplegia or hemiplegia also have altered growth [7].

L’incidence et la gravité de la malnutrition des enfants ayant une DN sont proportionnelles à la durée et la gravité de leur déficience.[7][11][12] La croissance des enfants ayant une quadriplégie spastique est plus touchée, mais celle des enfants diplégiques ou hémiplégiques en souffre également [7].




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Date index:2022-10-16 -

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