Pereira Daniela Cardoso, Bussamra Luiz Claudio Silva, Araujo Júnior Edward, Drummond Carolina Leite, Nardozza Luciano Marcondes Machado, Moron Antonio Fernandes, Aldrighi José Mendes
Department of Obstetrics and Gynecology, School of Medical Sciences, Santa Casa de São Paulo (FCMSCSP), São Paulo, SP, Brazil.
Case Rep Obstet Gynecol. 2013;2013:203976. doi: 10.1155/2013/203976. Epub 2013 Apr 4.
Treacher-Collins syndrome (TCS) is a rare dominant autosomal anomaly resulting from malformation or disruption of the development of the first and second branchial arches. It is characterized by micrognathia, malar hypoplasia, and malformations of the eyes and ears. The prenatal diagnosis using two-dimensional ultrasonography (2DUS) is characterized by identification of facial malformations together with polyhydramnios. Three-dimensional ultrasonography (3DUS) has the capacity to spatially display these facial malformations, thus making it easy for the parents to understand them. We present a case of TCS diagnosed in the 33rd week using 3DUS, with postnatal confirmation using cranial computed tomography and anatomopathological analysis.
特雷彻 - 柯林斯综合征(TCS)是一种罕见的常染色体显性异常疾病,由第一和第二鳃弓发育畸形或发育中断引起。其特征为小颌畸形、颧骨发育不全以及眼耳畸形。二维超声检查(2DUS)进行产前诊断的特点是可识别面部畸形并伴有羊水过多。三维超声检查(3DUS)能够在空间上显示这些面部畸形,从而便于父母理解。我们报告一例在孕33周时通过3DUS诊断出的TCS病例,并通过头颅计算机断层扫描和解剖病理学分析进行产后确诊。