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Afocal ocular
Alport's syndrome
Familial hereditary nephropathy
Greig hypertelorism
Greig's syndrome
Haematuric familial nephropathy
Hereditary nephropathy
Hereditary nephropathy with haematuria
Hypertelorism
Non-corrective ocular
Ocular hypertelorism
Ocular motoricity
Ocular motricity
Orbital hypertelorism
Plano ocular
Total ocular motility

Translation of "ocular 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


total ocular motility [ ocular motoricity | ocular motricity ]

oculomotricité
The Eye
Oeil


afocal ocular [ plano ocular | non-corrective ocular ]

oculaire afocal [ oculaire plan | oculaire non correcteur ]
Optical Glass | The Eye
Verres d'optique | Oeil


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


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


Greig hypertelorism

hypertélorisme de Greig
IATE - Health
IATE - Health


hypertelorism

hypertélorisme
médecine > anatomopathologie
médecine > anatomopathologie


hereditary nephropathy | Alport's syndrome | hereditary haematuria associated with nerve deafness and ocular changes | hereditary hematuria associated with nerve deafness and ocular changes | hereditary nephropathy with haematuria | familial hereditary nephropathy | haematuric familial nephropathy

néphropathie familiale avec surdité | syndrome d'Alport | néphrite hématurique héréditaire avec surdité | néphrite chronique héréditaire
médecine > néphrologie et urologie
médecine > néphrologie et urologie




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'ocular hypertelorism'

Date index:2022-10-18 -

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