医学
羊水过多
特雷彻-柯林斯综合征
产前诊断
子宫内
解剖
颅面
怀孕
胎儿
遗传学
精神科
生物
作者
Sayo Kubo,Takashi Horinouchi,Masahiro Kinoshita,Toshiyuki Yoshizato,Yutaka Kozuma,Takaaki Shinagawa,Kimio Ushijima
标识
DOI:10.1016/j.tjog.2019.05.024
摘要
We present a case with prenatal diagnosis of Treacher-Collins syndrome in which micrognathia and other facial and ear abnormalities were described using a three- and four-dimensional (3D/4D) ultrasonography in utero. A 39-year-old Japanese pregnant woman was referred because of polyhydramnios at 29 weeks' gestation. Conventional ultrasonography showed a hypoplastic mandible on the sagittal section of fetal head. Continuous observation using a 3D ultrasonography additionally demonstrated bilateral downslanting palpebral fissures with symmetry and macrostomia as well as micrognathia. Both ears were microtia and no polydactyly or missing fingers were found. The advantage of the rendering mode of 3D images covering entire face including ears and limbs was enhanced by a continuous observation, so called 4D ultrasonography, under a condition of polyhydramnios, providing visual diagnosis in utero.
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