Prenatal Diagnosis of Pentalogy of Cantrell with Increased Nuchal Translucency: Case Report

Authors

  • Deniz Cemgil Arıkan Kahramanmaraş Sütçü İmam University Medical Faculty Department of Obstetrics and Gynecology, Kahramanmaras
  • Semih Yancar Kahramanmaraş Sütçü İmam University Medical Faculty Department of Obstetrics and Gynecology, Kahramanmaras
  • Fethi Güçer Kahramanmaraş Sütçü İmam University Medical Faculty Department of Obstetrics and Gynecology, Kahramanmaras
  • Ender Zencir Kahramanmaraş Sütçü İmam University Medical Faculty Department of Obstetrics and Gynecology, Kahramanmaras
  • Hakan Beyazıt Kahramanmaras State Hospital, Department of Obstetrics and Gynecology, Kahramanmaraş

Keywords:

Pentalogy of Cantrell, Increased nuchal translucency, Omphalocele, Prenatal diagnosis

Abstract

Pentalogy of Cantrell is a rare sporadic syndrome with unknown etiology. We aimed to present a prenatally diagnosed case of pentalogy of Cantrell associated with increased nuchal translucency (NT). A twenty-two year old G2P0A1 pregnant woman was admitted to our clinic for routine prenatal ultrasonographic scanning at 14th weeks of gestation. Ultrasound scan revealed a NT of 7.9 mm and a large omphalocele containing the liver, bowel, and heart with ventricular septal defect. After taking the written informed consent form the parents the pregnancy was terminated. Postmortem examination confirmed the ultrasound findings and chromosome analysis revealed a normal karyotype. Increased NT measurement
in first trimester of pregnancy may also bring the fetus to early attention for pentology of Cantrell if an omphalocele associates with this condition.

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Published

2011-12-10

How to Cite

1.
Arıkan DC, Yancar S, Güçer F, Zencir E, Beyazıt H. Prenatal Diagnosis of Pentalogy of Cantrell with Increased Nuchal Translucency: Case Report. Gynecol Obstet Reprod Med [Internet]. 2011Dec.10 [cited 2024Apr.19];17(3):173-6. Available from: https://gorm.com.tr/index.php/GORM/article/view/319

Issue

Vol. 17 No. 3 (2011)

Section

Case Reports

License

CC BY

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