Mégarbané A, Haddad S, Berjaoui L
Unité de Génétique Médicale, Faculté de Médecine, Université Saint-Joseph, Beirut, Lebanon.
Am J Perinatol. 1998 Jul;15(7):403-7. doi: 10.1055/s-2007-993966.
Fibrochondrogenesis, a rare lethal chondrodysplasia has been reported on nine patients. We report on a boy with fibrochondrogenesis whose parents were second cousins. Prenatal ultrasonography performed at 22 weeks of gestation revealed an intrauterine growth retardation, an apparently large head, an hypoplasia of the thorax, a prominent abdomen, rhizomelic limbs, and wide metaphysis. The latest have never been reported in other lethal dysplasias.
纤维软骨发育异常是一种罕见的致死性软骨发育不良,已有9例相关报道。我们报告了一名患有纤维软骨发育异常的男孩,其父母为近亲(表亲)。妊娠22周时进行的产前超声检查显示胎儿宫内生长迟缓、头部明显较大、胸廓发育不全、腹部突出、肢体近端短小以及干骺端增宽。后者在其他致死性发育不良中从未有过报道。