Literature DB >> 12868086

Prenatal diagnosis of 5p deletion syndrome following abnormally low maternal serum human chorionic gonadotrophin.

Amir Weiss1, Stavit Shalev, Ehud Weiner, Yona Shneor, Eliezer Shalev.   

Abstract

Prenatal diagnosis of 5p deletion syndrome, or cri du chat, following an abnormally low measurement of a screening of serum human chorionic gonadotrophin (hCG), is reported. Karyotyping following amniocentesis revealed a terminal deletion in the short arm of one chromosome 5. The pregnancy was electively terminated. 5p deletion syndrome has been described with abnormally high hCG levels and normal hCG levels. This is the first report of its association with abnormally low levels. The association between chromosomal abnormalities and hCG is discussed. Copyright 2003 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12868086     DOI: 10.1002/pd.645

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  5 in total

Review 1.  5p deletions: Current knowledge and future directions.

Authors:  Joanne M Nguyen; Krista J Qualmann; Rebecca Okashah; AmySue Reilly; Mikhail F Alexeyev; Dennis J Campbell
Journal:  Am J Med Genet C Semin Med Genet       Date:  2015-08-03       Impact factor: 3.908

Review 2.  Cri du Chat syndrome.

Authors:  Paola Cerruti Mainardi
Journal:  Orphanet J Rare Dis       Date:  2006-09-05       Impact factor: 4.123

3.  Discordance for Cri du Chat Syndrome in a dichorionic-diamniotic twin pregnancy.

Authors:  Mireia González-Comadran; José Luís Hernández Sánchez; Carolina Rueda; Elena Ferriols; Maria Prat; Ricardo Rubio; Ramón Carreras
Journal:  Case Rep Womens Health       Date:  2015-07-29

4.  Prenatal Sonographic Features of Cri-du-Chat Syndrome: A Case Report and Analytical Literature Review.

Authors:  Kuntharee Traisrisilp; Yuri Yanase; Srimeunwai Ake-Sittipaisarn; Theera Tongsong
Journal:  Diagnostics (Basel)       Date:  2022-02-06

5.  Prenatal diagnosis of cri-du-chat syndrome by SNP array: report of twelve cases and review of the literature.

Authors:  Jiasun Su; Huayu Fu; Bobo Xie; Weiliang Lu; Wei Li; Yuan Wei; Qiang Zhang; Shengkai Wei; Qiuli Chen; Yingchi Lu; Tingting Jiang; Jingsi Luo; Zailong Qin
Journal:  Mol Cytogenet       Date:  2019-12-09       Impact factor: 2.009

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.