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Blitz-Nick-Salaam-Krämpfe
Eclampsia nutans
Epilepsy syndrome
Familial spastic paralysis
Flatfoot
Flexion spasm
Generalized flexion epilepsy syndrome
HSP
Hereditary spastic paraplegia
Infantile spasm
Infantile spastic epilepsy
Infantile spastic hemiplegia
Jackknife spa
Nodding spasm
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
Spasticity
Strümpell's disease
West syndrome

Vertaling van "Spastic flatfoot " (Engels → Frans) :

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

pied plat spastique


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 ]


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

paraplégie spastique familiale [ maladie de Strümpell-Lorrain | paraplégie spasmodique familiale de Strümpell-Lorrain ]


infantile spastic hemiplegia | spastic hemiplegia

h.spasmodique infantile | hémiplégie spasmodique




Congenital spastic paralysis (cerebral) Spastic cerebral palsy NOS

Paralysie cérébrale spastique SAI


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


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


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

syndrome d'ataxie spastique-epilepsie myoclonique-neuropathie précoce






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'Spastic flatfoot' ->

Date index: 2023-07-08
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