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Anhidrotic ectodermal dysplasia
Canadian Society for Ectodermal Dysplasias
Chondroectodermal dysplasia
Christ-Siemens syndrome
Christ-Siemens-Touraine syndrome
Cleidocranial dysostosis
Cleidocranial dysplasia
Craniometaphyseal dysplasia
EVC
Ellis-van Creveld syndrome
Hereditary ectodermal dysplasia
Hypogonadism with anosmia
Kallmann syndrome
Kallmann's syndrome
Mesoectodermal dysplasia
Metaphyseal dysplasia
Olfactory genital dysplasia
Parietal foramina with cleidocranial dysplasia
Pyle's disease

Traduction de «Cleidocranial dysplasia » (Anglais → Français) :

cleidocranial dysostosis [ cleidocranial dysplasia ]

dysostose cléïdo-crânienne [ dysplasie cléïdo-crânienne | dysostose cléïdo-crânienne héréditaire | syndrome de Pierre-Marie, Foy et Sainton ]


cleidocranial dysostosis,cleidocranial dysplasia

dysostose cléidocrânienne | dysplasie cléidocrânienne | hydrocéphalie héréditaire | maladie de Marie et Sainton | syndrome de Scheuthauer


Parietal foramina with cleidocranial dysplasia

foramen pariétal avechypoplasie claviculaire


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


craniometaphyseal dysplasia | metaphyseal dysplasia | Pyle's disease

dysplasie crânio-métaphysaire familiale | dysplasie métaphysaire familiale | maladie de Pyle


chondroectodermal dysplasia | Ellis-van Creveld syndrome | mesoectodermal dysplasia | EVC [Abbr.]

chondrodysplasie chondroectodermique | syndrome d'Ellis-van Creveld


A rare genetic immuno-osseous dysplasia disorder with characteristics of pre and post-natal growth retardation, hypotonia, borderline to moderate intellectual disability, retinal dystrophy, spondyloepiphyseal dysplasia (epiphyseal dysplasia, epiphyse

syndrome de Roifman


Canadian Society for Ectodermal Dysplasias

Canadian Society for Ectodermal Dysplasias


Kallmann's syndrome [ hypogonadism with anosmia | Kallmann syndrome | olfactory genital dysplasia ]

dysplasie olfactogénitale [ syndrome de Morsier-Kallmann | dysplasie olfacto-génitale | syndrome de Morsier ]


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


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