Socolov R, Rusu Cristina, Socolov Demetra, Iliev G, Buţureanu St, Covali Roxana
"Gr.T. Popa" University of Medicine and Pharmacy Iaşi, School of Medicine, Department of Obstetrics and Gynecology.
Rev Med Chir Soc Med Nat Iasi. 2006 Jan-Mar;110(1):144-7.
The authors present the case of a foetus with Jeune syndrome (asphyxiating thoracic dystrophy) in a woman with a previous deceased child with the same disease, and also with a normal sibling. The diagnosis was mentioned at 26 week of pregnancy, based on ultrasonographic findings: short proximal bones (under 3 percentiles), and a diminished thoracic circumference, (although greater than 10 percentiles for the gestational age). There was an interdisciplinary agreement for the therapeutic termination of the pregnancy, and the post-expulsion assessment confirmed the diagnosis. This case demonstrates a higher incidence of Jeune dystrophy than the one expected for an autosomal recessive disease, with 2 out of 3 children affected, instead of 25%. It also shows that the earliest change is the one regarding the shortened long bones, often difficult to notice before 20 weeks, fact which favors a detailed genetic sonogram done after this limit.