Picone O, Brisset S, Senat M-V, Maurin M-L, Frydman R, Tachdjian G
Inserm U-782, service de gynécologie-obstétrique, hôpital Antoine-Béclère, AP-HP, université Paris-Sud, UMR-S0782, 157, rue de la Porte-de-Trivaux, 92140 Clamart, France.
J Gynecol Obstet Biol Reprod (Paris). 2008 May;37(3):299-301. doi: 10.1016/j.jgyn.2007.11.001. Epub 2007 Dec 21.
We present a rare case of prenatal diagnosis of two de novo chromosome structural rearrangements including a translocation (1;3) associated with a 22q11.2 deletion. The amniocentesis was performed because the systematic ultrasound examination revealed: right aortic cross with double aortic arch, with normal size of aorta and pulmonary artery. Our report emphasises that 22q11.2 deletion must be looked for when a fetal cardiac conotruncal malformation is diagnosed, even in the presence of another chromosomal abnormality. In prenatal diagnosis, this can have implication for patient management and genetic counselling.
我们报告了一例罕见的产前诊断出两种新发染色体结构重排的病例,其中包括与22q11.2缺失相关的(1;3)易位。进行羊膜穿刺术是因为系统超声检查发现:右位主动脉弓伴双主动脉弓,主动脉和肺动脉大小正常。我们的报告强调,即使存在另一种染色体异常,当诊断出胎儿心脏圆锥动脉干畸形时,也必须查找22q11.2缺失。在产前诊断中,这可能对患者管理和遗传咨询有影响。