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