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Diplegia
Familial spastic paralysis
HSP
Hereditary spastic paraplegia
Infantile spastic hemiplegia
Little's disease
Peroneal spastic flat foot
Peroneal spastic flatfoot
Spasmodic flat foot
Spasmodic flatfoot
Spasmodic talipes planus
Spastic diplegia
Spastic flat foot
Spastic flatfoot
Spastic hemiplegia
Strümpell's disease

Traduction de «Spastic diplegia » (Anglais → Français) :

Little's disease [ spastic diplegia ]

maladie de Little [ diplégie spastique ]


Little's disease | spastic diplegia

diplégie spastique infantile | maladie de Little | syndrome de Little


Symmetrical thalamic calcifications are clinically distinguished by a low Apgar score, spasticity or marked hypotonia, weak or absent cry, poor feeding and facial diplegia or weakness. It is an extremely rare condition, with about 30 cases described

calcifications thalamiques symétriques


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

pied plat spastique


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




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

syndrome d'ataxie spastique-epilepsie myoclonique-neuropathie précoce


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






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'Spastic diplegia' ->

Date index: 2022-12-30
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