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[Antenatal diagnosis of achondrogenesis. Two successive cases in the same family]. / Diagnostic anténatal de l'achondrogenèse. A propos de deux cas successifs dans une même fratrie.
Boudier, E; Zurlinden, B; Cour, A; Rognon, M; Devalland-Monnin, C; Nirhy-Lanto, A; el Khadissi, H.
Afiliação
  • Boudier E; Service de Gynécologie-Obstétrique, Centre Hospitalier Général, Montbéliard.
Article em Fr | MEDLINE | ID: mdl-1955657
ABSTRACT
Achondrogenesis is a rare case of fetal skeletal dysplasia. Achondrogenesis in lethal. That is a autosomal recessive fetal skeletal dysplasia. There is a very important dwarfism with extreme micromely, macrocephalia and brevity of chest. The authors enumerate the echographics, radiologics and histologics symptoms of this chondro-dysplasia. The authors comment rapidly the others diagnosis of lethal fetal skeletal dysplasia. Genetic consul is a necessity.
Assuntos
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Base de dados: MEDLINE Assunto principal: Ultrassonografia Pré-Natal / Nanismo / Doenças Genéticas Inatas Idioma: Fr Ano de publicação: 1991 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Ultrassonografia Pré-Natal / Nanismo / Doenças Genéticas Inatas Idioma: Fr Ano de publicação: 1991 Tipo de documento: Article