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10号染色体长臂末端三体胎儿的产前诊断

Prenatal diagnosis of a fetus with distal 10q trisomy.

作者信息

Chen C P, Shih J C, Lee C C, Chen L F, Wang W, Wang T Y

机构信息

Department of Obstetrics and Gynecology, Mackay Memorial Hospital, Taipei, Taiwan, R.O.C.

出版信息

Prenat Diagn. 1999 Sep;19(9):876-8. doi: 10.1002/(sici)1097-0223(199909)19:9<876::aid-pd651>3.0.co;2-8.

Abstract

Distal 10q trisomy is a well-defined but rare syndrome. Most cases are diagnosed in infancy or in childhood and rarely include prenatal findings. We present a case of fetal distal 10q trisomy with abnormal prenatal sonographic findings. A 19-year-old primigravida was referred for genetic counselling at 18 gestational weeks because her husband had a familial history of congenital anomalies. Genetic amniocentesis was thus performed and showed fetal distal 10q trisomy (10q24.1-->qter), 46,XX,der(22)t(10;22)(q24.1;p11.2)pat, resulting from paternal t(10;22) reciprocal translocation. Level II ultrasonograms further demonstrated bilateral hydronephrosis, ventricular septal defect and facial dysmorphism ascertained by three-dimensional ultrasound. The pregnancy was terminated at 22 gestational weeks. Post-mortem autopsy confirmed the sonographic findings. We suggest that abnormal prenatal sonographic findings such as cardio-vascular, renal and facial malformations should alert cytogeneticists to search for subtle chromosomal abnormalities.

摘要

10号染色体长臂远端三体综合征是一种明确但罕见的综合征。大多数病例在婴儿期或儿童期被诊断出来,产前发现的情况很少见。我们报告一例胎儿10号染色体长臂远端三体综合征,伴有异常的产前超声检查结果。一名19岁的初产妇在孕18周时因丈夫有先天性畸形家族史而前来接受遗传咨询。因此进行了遗传羊水穿刺检查,结果显示胎儿为10号染色体长臂远端三体(10q24.1→qter),核型为46,XX,der(22)t(10;22)(q24.1;p11.2)pat,由父亲的t(10;22)相互易位导致。二级超声检查进一步显示双侧肾积水、室间隔缺损以及通过三维超声确定的面部畸形。该孕妇在孕22周时终止妊娠。尸检证实了超声检查结果。我们建议,产前超声检查发现的如心血管、肾脏和面部畸形等异常情况应提醒细胞遗传学家去寻找细微的染色体异常。

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