Vertaling van "skeletal dysplasia " (Engels → Frans) :

skeletal dysplasia
dysplasie osseuse

A lethal skeletal dysplasia with characteristics of cloverleaf skull anomaly, facial dysmorphism, limb shortness, splenic hypo/aplasia and radiological anomalies including thin tubular bones with flared metaphyses and deficient calvarial mineralisati
ostéocraniosténose

Omodysplasia is a rare skeletal dysplasia characterised by severe limb shortening and facial dysmorphism. Two types of omodysplasia have been described: an autosomal recessive or generalised form (also referred to as micromelic dysplasia with disloca
omodysplasie

A rare familial skeletal dysplasia with characteristics of multiple epiphyseal dysplasia with extremely retarded ossification. It has been described in 6 members of a unique consanguineous family. A mutation in PTHR1 gene is responsible for this synd
syndrome d'Eiken

anhidrotic ectodermal dysplasia | Christ-Siemens syndrome | hereditary ectodermal dysplasia | Christ-Siemens-Touraine syndrome
dysplasie ectodermique anhidrotique | dysplasie ectodermique | syndrome de Christ-Siemens | syndrome de Christ-Siemens-Touraine

multiple epiphyseal dysplasia | M.E.D. | MED | Multiple Epiphyseal Dysplasia
dysplasies épiphysaires multiples | dysplasies polyépiphysaires

hip dysplasia | dysplasia of hip
dysplasie de la hanche

Skeletal Street Network File [ Skeletal Street Network Files ]
Fichier schématique du réseau routier

chondroectodermal dysplasia | Ellis-van Creveld syndrome | mesoectodermal dysplasia | EVC [Abbr.]
chondrodysplasie chondroectodermique | syndrome d'Ellis-van Creveld

craniometaphyseal dysplasia | metaphyseal dysplasia | Pyle's disease
dysplasie crânio-métaphysaire familiale | dysplasie métaphysaire familiale | maladie de Pyle