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Blitz-Nick-Salaam-Krämpfe
Eclampsia nutans
Epilepsy syndrome
Familial spastic paralysis
Flexion spasm
Generalized flexion epilepsy syndrome
HSP
Hereditary spastic paraplegia
Infantile spasm
Infantile spastic epilepsy
Infantile spastic hemiplegia
Jackknife spa
Nodding spasm
Paraplegia
Peroneal spastic flat foot
Peroneal spastic flatfoot
Salaam attack
Salaam convulsion
Salaam seizure
Spasmodic flat foot
Spasmodic flatfoot
Spasmodic talipes planus
Spastic flat foot
Spastic flatfoot
Spastic hemiplegia
Strümpell's disease
Tropical spastic paraplegia
West syndrome

Translation of "Spastic paraplegia " (English → French) :

Tropical spastic paraplegia

Paraplégie spastique tropicale
WORLD HEALTH ORGANIZATION ICD-10: G04.1
WORLD HEALTH ORGANIZATION ICD-10: G04.1


hereditary spastic paraplegia [ HSP | familial spastic paralysis | Strümpell's disease ]

paraplégie spastique familiale [ maladie de Strümpell-Lorrain | paraplégie spasmodique familiale de Strümpell-Lorrain ]
Nervous System | Human Diseases - Various
Système nerveux | Maladies humaines diverses


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


hereditary spastic paraplegia

maladie de Strümpell-Lorrain | paraplégie spasmodique familiale | paraplégie spastique familiale
IATE - Health
IATE - Health


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


spastic flatfoot [ spastic flat foot | spasmodic flatfoot | spasmodic flat foot | spasmodic talipes planus | peroneal spastic flatfoot | peroneal spastic flat foot ]

pied plat spastique
Musculoskeletal System | Symptoms (Medicine)
Appareil locomoteur (Médecine) | Symptômes (Médecine)


infantile spasm [ West syndrome | nodding spasm | salaam convulsion | salaam seizure | salaam attack | generalized flexion epilepsy syndrome | epilepsy syndrome | Blitz-Nick-Salaam-Krämpfe | eclampsia nutans | flexion spasm | infantile spastic epilepsy | infantile spastic epilepsy | jackknife spa ]

spasme infantile [ syndrome de West | spasme en flexion | tic de salaam | syndrome des spasmes en flexion | épilepsie en flexion généralisée | encéphalite myoclonique infantile avec hypsarythmie | spasmus nutans ]
Nervous System | Symptoms (Medicine)
Système nerveux | Symptômes (Médecine)


infantile spastic hemiplegia | spastic hemiplegia

h.spasmodique infantile | hémiplégie spasmodique
IATE - Health
IATE - Health






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'Spastic paraplegia'

Date index:2022-02-25 -

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