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Greig hypertelorism
Greig's syndrome
Hypertelorism
Ocular hypertelorism
Orbital hypertelorism

Translation of "hypertelorism " (English → French) :

ocular hypertelorism [ orbital hypertelorism ]

hypertélorisme oculaire
Visual Disorders | The Eye | Musculoskeletal System
Troubles de la vision | Oeil | Appareil locomoteur (Médecine)


ocular hypertelorism | hypertelorism | Greig's syndrome

hypertélorisme oculaire | hypertélorisme | syndrome de Greig
médecine > anatomopathologie | médecine > ophtalmologie
médecine > anatomopathologie | médecine > ophtalmologie


hypertelorism

hypertélorisme
IATE - Health
IATE - Health


Greig hypertelorism

hypertélorisme de Greig
IATE - Health
IATE - Health


hypertelorism

hypertélorisme
médecine > anatomopathologie
médecine > anatomopathologie


Hypertelorism

Hypertélorisme
WORLD HEALTH ORGANIZATION ICD-10: Q75.2
WORLD HEALTH ORGANIZATION ICD-10: Q75.2


A rare multiple congenital anomalies syndrome with characteristics of mild intellectual disability, short stature, cardiac anomalies, mild dysmorphic features (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlax

syndrome cranio-facio-fronto-digital
SNOMEDCT-BE (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlax / 763320005
SNOMEDCT-BE (disorder) / 763320005


A rare neurologic disease characterized by global developmental delay, intellectual disability, multiple ischemic lesions on brain MRI, behavioral abnormalities, dystonia, choreic movements and pyramidal syndrome, facial dysmorphism (hypertelorism, a

syndrome autosomique récessif de leucoencéphalopathie-infarctus cérébraux-rétinite pigmentaire
SNOMEDCT-BE (hypertelorism, a / 771476007
SNOMEDCT-BE (disorder) / 771476007


A rare chromosomal anomaly syndrome with principle characteristics of intrauterine growth restriction, congenital cardiac anomalies (ventricular and atrial septal defects, patent ductus arteriosus) and craniofacial dysmorphism (hypertelorism, downsla

trisomie 15 en mosaïque
SNOMEDCT-BE (ventricular and atrial septal defects, patent ductus arteriosus) and craniofacial dysmorphism (hypertelorism, downsla / 764619001
SNOMEDCT-BE (disorder) / 764619001




Others have searched : greig hypertelorism    greig's syndrome    hypertelorism    ocular hypertelorism    orbital hypertelorism    


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'hypertelorism'

Date index:2023-12-20 -

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