Literature DB >> 16095036

A rare case of interstitial del(1)(p34.3p36.11) diagnosed prenatally.

Hua Yang1, Christine L Y Lee, David C Young, Michelle Shortliffe, Weiming Yu, James R Wright.   

Abstract

We report a very rare constitutional interstitial deletion of chromosome 1p defined within 1p34.3-36.11 bands with an intact pter. The diagnosis was made by standard cytogenetics and fluorescence in situ hybridization (FISH) studies on a cordocentesis specimen obtained at 21 weeks gestation. Termination of pregnancy was performed at 22 weeks gestation due to the ultrasound diagnosis of congenital heart disease. Autopsy confirmed congenital heart disease (cardiomegaly, Ebstein's anomaly, secundum atrial septal defect, subendocardial fibroelastosis), pulmonary lymphangiectasis, a high arched palate, short neck, and bilateral long proximally implanted thumbs. To our knowledge, this is the first case of del(1) (p34.3p36.11) diagnosed prenatally.

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Year:  2004        PMID: 16095036     DOI: 10.1080/15227950490923624

Source DB:  PubMed          Journal:  Fetal Pediatr Pathol        ISSN: 1551-3815            Impact factor:   0.958


  2 in total

1.  Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7.

Authors:  K van Engelen; A V Postma; J B A van de Meerakker; J W Roos-Hesselink; A T J M Helderman-van den Enden; H W Vliegen; T Rahman; M J H Baars; J-W Sels; U Bauer; T Pickardt; S R Sperling; A F M Moorman; B Keavney; J Goodship; S Klaassen; B J M Mulder
Journal:  Neth Heart J       Date:  2013-03       Impact factor: 2.380

2.  Prenatal diagnosis of 1p34.3 interstitial microdeletion by aCGH in a fetus with jaw bone abnormalities.

Authors:  Themistoklis Dagklis; Elena Papageorgiou; Elisavet Siomou; Vassilis Paspaliaris; Christina Zerva; Panagiotis Chatzis; Loretta Thomaidis; Emmanouil Manolakos; Ioannis Papoulidis
Journal:  Mol Cytogenet       Date:  2016-10-06       Impact factor: 2.009

  2 in total

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