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Abnormal movement
Abnormal movement of head
Abnormal movements clinic
Complet abnormal movement
Complete a movement

Translation of "complet abnormal movement " (English → French) :

complet abnormal movement

mouvement généralisé anormal
IATE - Health
IATE - Health


abnormal movement

mouvement anormal
Musculoskeletal System | Symptoms (Medicine)
Appareil locomoteur (Médecine) | Symptômes (Médecine)


abnormal movements clinic

service de consultation pour dyskinésies
Health Institutions
Établissements de santé


abnormal movement

désordre moteur
IATE - Health
IATE - Health


abnormal movement of head

mouvement anormal de la tête
IATE - Health
IATE - Health


complete a movement

exécuter un mouvement
Rail Transport
Transport par rail


O/E - bone-abnormal movement

à l'examen : mouvement anormal d'un os
SNOMEDCT-CA (constatation) / 164594008
SNOMEDCT-CA (constatation) / 164594008


Abnormal movement

mouvement anormal
SNOMEDCT-CA (constatation) / 225606002
SNOMEDCT-CA (constatation) / 225606002


An extremely rare syndrome described in three members of a family (a mother and her two children) with the association of various ocular abnormalities (partial or complete aniridia, ptosis, pendular nystagmus, corneal pannus, persistent pupillary mem

syndrome d'aniridie-ptosis-déficience intellectuelle-obésité
SNOMEDCT-BE (a mother and her two children) with the association of various ocular abnormalities (partial or complete aniridia, ptosis, pendular nystagmus, corneal pannus, persistent pupillary mem / 720987001
SNOMEDCT-BE (disorder) / 720987001


Definition: A condition, so far found only in girls, in which apparently normal early development is followed by partial or complete loss of speech and of skills in locomotion and use of hands, together with deceleration in head growth, usually with an onset between seven and 24 months of age. Loss of purposive hand movements, hand-wringing stereotypies, and hyperventilation are characteristic. Social and play development are arres ...[+++]

Définition: Trouble décrit jusqu'ici uniquement chez les filles, caractérisé par un développement initial apparemment normal, suivi d'une perte partielle ou complète du langage, de la marche, et de l'usage des mains, associé à un ralentissement du développement crânien et survenant habituellement entre 7 et 24 mois. La perte des mouvements volontaires des mains, les mouvements stéréotypés de torsion des mains et une hyperventilation, sont caractéristiques de ce trouble. Le ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: F84.2
WORLD HEALTH ORGANIZATION ICD-10: F84.2




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'complet abnormal movement'

Date index:2021-12-15 -

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