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猫叫综合征:临床特征与产前诊断

Cri-du-chat syndrome: clinical profile and prenatal diagnosis.

作者信息

Tullu M S, Muranjan M N, Sharma S V, Sahu D R, Swami S R, Deshmukh C T, Bharucha B A

机构信息

Department of Paediatrics, Seth G.S. Medical College, Mumbai.

出版信息

J Postgrad Med. 1998 Oct-Dec;44(4):101-4.

Abstract

Prenatal diagnosis of cri-du-chat syndrome is described in 2 pregnancies. In Case 1, the mother was a balanced translocation carrier and had 2 previously affected off springs. Prenatal diagnosis by chorion villus sampling and cordocentesis was successful in diagnosing an affected conceptus and the pregnancy was electively terminated. Case 2 was referred for nonimmune foetal hydrops and cordocentesis revealed deletion 5p. This second case was noteworthy for the fact that deletion 5p has not been reported to cause foetal hydrops.

摘要

本文描述了2例猫叫综合征的产前诊断病例。病例1中,母亲是平衡易位携带者,之前有2个患病子女。通过绒毛取样和脐带穿刺进行产前诊断,成功诊断出一个患病胎儿,该妊娠被选择性终止。病例2因非免疫性胎儿水肿转诊,脐带穿刺显示5p缺失。第二例值得注意的是,此前尚未有报道称5p缺失会导致胎儿水肿。

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