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Congenital deformity of clavicle
Congenital high scapula
Dislocation of elbow
Elbow
Forearm
Scapula
Scapula elevata
Shoulder
Sprengel shoulder
Sprengel's deformity

Translation of "Congenital high scapula " (English → French) :

Sprengel's deformity [ congenital high scapula | scapula elevata | Sprengel shoulder ]

surélévation congénitale de l'omoplate [ S.C.O. | élévation congénitale de l'omoplate | déformation de Sprengel | syndrome de Sprengel | malformation de Sprengel | scapula elevata ]
Bones and Joints | Musculoskeletal System | Symptoms (Medicine)
Os et articulations | Appareil locomoteur (Médecine) | Symptômes (Médecine)


Sprengel's deformity | congenital high scapula | scapula elevata

malformation de Sprengel | surélévation congénitale de l'omoplate
biologie > embryologie | biologie > génétique | médecine > sémiologie et pathologie
biologie > embryologie | biologie > génétique | médecine > sémiologie et pathologie


A multiple congenital anomalies syndrome characterized by moderate postnatal overgrowth, macrocephaly, craniofacial dysmorphism (including high forehead and anterior hairline, downslanting palpebral fissures, prominent chin), developmental delay, and

syndrome de croissance excessive de Malan
SNOMEDCT-BE (including high forehead and anterior hairline, downslanting palpebral fissures, prominent chin), developmental delay, and / 763795006
SNOMEDCT-BE (disorder) / 763795006


A rare genetic congenital hypothyroidism disorder with characteristics of mild global developmental delay in childhood, short stature, delayed bone age and abnormal thyroid and selenium levels in serum (high total and free T4 concentrations, low T3,

petite taille-retard d'âge osseux par déficit du métabolisme de l'hormone thyroïdienne
SNOMEDCT-BE (high total and free T4 concentrations, low T3, / 763890006
SNOMEDCT-BE (disorder) / 763890006


Congenital:deformity of:clavicle | elbow | forearm | scapula | dislocation of:elbow | shoulder |

Anomalie morphologique congénitale de:avant-bras | clavicule | coude | omoplate | Luxation congénitale de:coude | épaule
WORLD HEALTH ORGANIZATION ICD-10: Q68.8
WORLD HEALTH ORGANIZATION ICD-10: Q68.8


Absence of uvula Congenital malformation of palate NOS High arched palate

Absence de luette Malformation congénitale du palais SAI Palais ogival
WORLD HEALTH ORGANIZATION ICD-10: Q38.5
WORLD HEALTH ORGANIZATION ICD-10: Q38.5


A rare congenital vascular anomaly syndrome characterized by venous or on occasion arterial malformations that lead to soft tissue hypertrophy and bone hypoplasia. An affected limb is generally shortened, highly deformed, painful and edematous with a

syndrome angio-ostéo-hypotrophique
SNOMEDCT-BE (disorder) / 765750001
SNOMEDCT-BE (disorder) / 765750001




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'Congenital high scapula'

Date index:2021-09-12 -

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