| Literature DB >> 12224076 |
Hanitra Randrianaivo1, Georges Haddad, Horatiu Roman, Anne Lise Delezoide, Annick Toutain, Martine Le Merrer, Claude Moraine, Anne Lise.
Abstract
Fibrochondrogenesis is a rare and lethal osteochondrodysplasia with an autosomal recessive mode of inheritance. We report a male fetus in which the diagnosis of lethal osteochondrodysplasia was suspected on prenatal ultrasound and radiological examinations during the second trimester of pregnancy. After termination of pregnancy, fibrochondrogenesis was diagnosed by radiological examination and histological study of fetal bones. Interwoven fibrous septa and fibroblastic degeneration of chondrocytes are pathognomonic. The recurrence rate is 25% and accurate diagnosis is necessary to enable genetic counselling. Copyright 2002 John Wiley & Sons, Ltd.Entities:
Mesh:
Year: 2002 PMID: 12224076 DOI: 10.1002/pd.423
Source DB: PubMed Journal: Prenat Diagn ISSN: 0197-3851 Impact factor: 3.050