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

作者信息

Boudier E, Zurlinden B, Cour A, Rognon M, Devalland-Monnin C, Nirhy-Lanto A, el Khadissi H

机构信息

Service de Gynécologie-Obstétrique, Centre Hospitalier Général, Montbéliard.

出版信息

J Gynecol Obstet Biol Reprod (Paris). 1991;20(5):623-6.

PMID: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.

摘要

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