[Antenatal diagnosis of achondrogenesis. Two successive cases in the same family]

Autor: E, Boudier, B, Zurlinden, A, Cour, M, Rognon, C, Devalland-Monnin, A, Nirhy-Lanto, H, el Khadissi
Jazyk: francouzština
Rok vydání: 1991
Předmět:
Zdroj: Journal de gynecologie, obstetrique et biologie de la reproduction. 20(5)
ISSN: 0368-2315
Popis: 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.
Databáze: OpenAIRE