The association of amelogenesis imperfecta and a microscopically typical hair dysplasia has been found in several members of a family in two generations. Transmission is X-linked.

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syndrome de trichodysplasie-amélogenèse imparfaite

SNOMEDCT-BE (disorder) / 719911000

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Amelogenesis imperfecta and gingival hyperplasia syndrome

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syndrome d'amélogénèse imparfaite-hyperplasie gingivale

SNOMEDCT-BE (disorder) / 707607008

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Amelogenesis | Dentinogenesis | Odontogenesis | imperfecta | Dentinal dysplasia Shell teeth

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Amelogenesis | Dentinogenesis | Odontogenesis | imperfecta | Dent en coquille Dysplasie de la dentine

WORLD HEALTH ORGANIZATION ICD-10: K00.5

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Others have searched : ai amelogenesis imperfecta amelogenesis dentinal dysplasia shell teeth dentinogenesis odontogenesis imperfecta

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'ai amelogenesis imperfecta'

Date index:2022-08-28 -

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Translation of "ai amelogenesis imperfecta " (English → French) :

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