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Angioma capillare et venosum calcificans
Angiomatosis meningo-oculofacialis
Bernard-Horner syndrome
Brevicollis
CRS
Claude Bernard-Horner syndrome
Congenital Horner syndrome
Congenital nephrosis
Congenital nephrotic syndrome
Congenital neuroectodermal dysplasia
Congenital osseous torticollis syndrome
Congenital rubella syndrome
Congenital synostosis of the cervicothoraci vertebrae
Congenital webbed neck syndrome
Cutaneocerebral angioma
Dimitri-disease
Encephalotrigeminal angiomatosis
Encephalotrigeminal syndrome
Familial nephrosis
Horner's oculopupillary syndrome
Horner's syndrome
Horner-Bernard syndrome
Kalischer's syndrome
Klippel-Feil anomaly
Klippel-Feil disease
Klippel-Feil sign
Klippel-Feil syndrome
Krabbe's II syndrome
Neurocutaneous syndrome
Parkes Weber's syndrome
Rubella syndrome
Sturge's disease
Sturge's syndrome
Sturge-Kalischer-Weber syndrome
Sturge-Weber disease
Sturge-Weber syndrome
Sturge-Weber-Dimitri syndrome
Weber-Dimitri syndrome

Traduction de «Congenital Horner syndrome » (Anglais → Français) :

Congenital Horner syndrome

syndrome de Horner congénital


Horner's syndrome [ Claude Bernard-Horner syndrome | Horner-Bernard syndrome | Bernard-Horner syndrome | Horner's oculopupillary syndrome ]

syndrome de Claude Bernard-Horner [ syndrome de Bernard-Horner | syndrome de Claude Bernard | syndrome de Horner | syndrome oculaire(-)sympathique | syndrome oculo-sympathique paralytique | syndrome oculo-sympathique | syndrome oculo-pupillaire ]


congenital nephrosis | familial nephrosis | congenital nephrotic syndrome

syndrome néphrotique congénital du nouveau-né


congenital rubella syndrome [ rubella syndrome ]

embryopathie rubéolique [ embryopathie rubéoleuse | syndrome de Gregg ]


Bernard-Horner syndrome

syndrome de Bernard | syndrome oculo-sympathique


congenital rubella syndrome | CRS [Abbr.]

embryofoetopathie rubéolique | embryopathie rubéoleuse | rubéole congénitale malformative | syndrome de Gregg | syndrome de rubéole congénitale


Rare syndrome with the association of congenital nephrotic syndrome, ocular anomalies and microcoria. The disorder results in proteinuria with nephrotic syndrome and histological lesions marked by diffuse mesangial sclerosis. Ocular anomalies are pre

syndrome de Pierson


A very rare multiple congenital anomalies syndrome described in three brothers of one South-African family, and with features of hypospadias and intellectual deficit, in association with microcephaly, craniofacial dysmorphism, joint laxity and beaked

syndrome d'hypospadias-déficience intellectuelle type Goldblatt


Klippel-Feil syndrome | Klippel-Feil anomaly | Klippel-Feil disease | Klippel-Feil sign | brevicollis | congenital osseous torticollis syndrome | congenital synostosis of the cervicothoraci vertebrae | congenital webbed neck syndrome

syndrome de Klippel-Feil | agénésie vertébrale cervicale | homme sans cou | syndrome de la réduction numérique cervicale


Sturge-Weber syndrome | Dimitri-disease | Kalischer's syndrome | Krabbe's II syndrome | Parkes Weber's syndrome | Sturge's syndrome | Sturge's disease | Sturge-Kalischer-Weber syndrome | Sturge-Weber disease | Sturge-Weber-Dimitri syndrome | Weber-Dimitri syndrome | angioma capillare et venosum calcificans | angiomatosis meningo-oculofacialis | congenital neuroectodermal dysplasia | cutaneocerebral angioma | encephalotrigeminal angiomatosis | encephalotrigeminal syndrome | neurocutaneous syndrome

syndrome de Sturge-Weber | angiomatose encéphalotrigéminée de Sturge-Weber-Krabbe | angiomatose méningo-oculo-faciale | angiomatose neuro-cutanée | angiomatose neuro-oculo-cutanée | maladie de Sturge-Weber-Krabbe | neuro-ectodermo-dysplasie congénitale | syndrome de Brushfield-Wyatt | syndrome neuro-cutané | syndrome de Parkes-Weber | syndrome de Sturge-Weber-Krabbe | syndrome de Weber-Dimitri


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