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

Burton skeletal dysplasia

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dysplasie squelettique de Burton

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skeletal dysplasia

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dysplasie osseuse

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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

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omodysplasie

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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

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syndrome d'Eiken

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Date index: 2021-12-19