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Angioma capillare et venosum calcificans
Angiomatosis meningo-oculofacialis
Buchmann and Meyer pattern
Buchmann-Meyer pattern
Christmas-tree pattern
Congenital neuroectodermal dysplasia
Craniometaphyseal dysplasia
Cutaneocerebral angioma
Dimitri-disease
Dysplasia epiphysealis hemimelica
Encephalotrigeminal angiomatosis
Encephalotrigeminal syndrome
Hypogonadism with anosmia
Kalischer's syndrome
Kallmann syndrome
Kallmann's syndrome
Krabbe's II syndrome
Light band width
Light-band pattern
Metaphyseal dysplasia
Meyer dysplasia of femoral head
Meyer's contrast experiment
Meyer's dysplasia
Meyer’s disease
Neurocutaneous syndrome
Olfactory genital dysplasia
Optical pattern
Parkes Weber's syndrome
Pyle's disease
Sturge's disease
Sturge's syndrome
Sturge-Kalischer-Weber syndrome
Sturge-Weber disease
Sturge-Weber syndrome
Sturge-Weber-Dimitri syndrome
Tarsoepiphyseal aclasis
Trevor's disease
Weber-Dimitri syndrome

Traduction de «Meyer's dysplasia » (Anglais → Français) :

Meyer’s disease | Meyer's dysplasia

dysplasie de Meyer




Meyer dysplasia of femoral head

dysplasie de la tête du fémur type Meyer


Buchmann and Meyer pattern | Buchmann-Meyer pattern | Christmas-tree pattern | light band width | light-band pattern | optical pattern

méthode de Buchmann et Meyer | méthode de la largeur du faisceau réfléchi


craniometaphyseal dysplasia | metaphyseal dysplasia | Pyle's disease

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


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


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


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

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


dysplasia epiphysealis hemimelica [ Trevor's disease | tarsoepiphyseal aclasis ]

dysplasie épiphysaire hémimélique [ syndrome de Trevor | aclasie tarso-épiphysaire | syndrome de Mouchet-Belot ]


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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