Literature DB >> 23981964

Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review.

Chih-Ping Chen1, Yi-Ning Su, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang.   

Abstract

We present rapid aneuploidy diagnosis of distal 9p deletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with an abnormal maternal serum screening result and intrauterine growth restriction (IUGR) in the fetus. We review the literature of prenatal diagnosis of distal 9p deletion, and add abnormal maternal serum biochemistry and fetal IUGR in the distinctive prenatal findings in pregnancy with fetal distal 9p deletion. We discuss the consequence of haploinsufficiency of DOCK8, KANK1, VLDLR and DMRT1 in this case.
© 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Array comparative genomic hybridization; Distal 9p deletion; Maternal serum screening; Prenatal diagnosis

Mesh:

Substances:

Year:  2013        PMID: 23981964     DOI: 10.1016/j.ygeno.2013.08.003

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  2 in total

1.  Copy number variation profile in the placental and parental genomes of recurrent pregnancy loss families.

Authors:  Laura Kasak; Kristiina Rull; Siim Sõber; Maris Laan
Journal:  Sci Rep       Date:  2017-03-27       Impact factor: 4.379

2.  From karyotypes to precision genomics in 9p deletion and duplication syndromes.

Authors:  Eleanor I Sams; Jeffrey K Ng; Victoria Tate; Ying-Chen Claire Hou; Yang Cao; Lucinda Antonacci-Fulton; Khadija Belhassan; Julie Neidich; Robi D Mitra; F Sessions Cole; Patricia Dickson; Jeffrey Milbrandt; Tychele N Turner
Journal:  HGG Adv       Date:  2021-12-24
  2 in total

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