Literature DB >> 26557571

Uncommon Presentation of Triploidy: A Case Report.

Işil Uzun1, Özlem Pata1, Cihat Unlu1, Fatma Tokat2, Mucize Ozdemir3.   

Abstract

A 28-year-old woman presented in her first pregnancy was admitted with severe hyperemesis gravidarium. Increased nuchal translucency with cardiac anomaly and omphalocele at the first trimester was observed at the ultrasound examination. Chorionic villus biopsy confirmed triploidy. The combination of type I and type II triploidy patterns were seen together in the second trimester of the pregnancy. Although the symptoms due to increased human chorionic levels occured, at the pathologic investigation there were no molar changes in the placenta. Here we report a case of uncommon presentation of triploidy.

Entities:  

Keywords:  Molar pregnancy; Nuchal translucency; Omphalocele

Year:  2015        PMID: 26557571      PMCID: PMC4625290          DOI: 10.7860/JCDR/2015/14037.6553

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


  8 in total

1.  Karyotype, phenotype and parental origin in 19 cases of triploidy.

Authors:  A Daniel; Z Wu; B Bennetts; H Slater; R Osborn; J Jackson; V Pupko; J Nelson; G Watson; C Cooke-Yarborough; C Loo
Journal:  Prenat Diagn       Date:  2001-12       Impact factor: 3.050

2.  Effects of triploidy on early human development.

Authors:  T Philipp; K Grillenberger; E R Separovic; K Philipp; D K Kalousek
Journal:  Prenat Diagn       Date:  2004-04       Impact factor: 3.050

3.  Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis.

Authors:  Paolo Guanciali-Franchi; Irene Iezzi; Barbara Matarrelli; Elisena Morizio; Giuseppe Calabrese; Giandomenico Palka
Journal:  Prenat Diagn       Date:  2010-08       Impact factor: 3.050

4.  Parental origin of triploidy in human fetuses: evidence for genomic imprinting.

Authors:  D E McFadden; L C Kwong; I Y Yam; S Langlois
Journal:  Hum Genet       Date:  1993-11       Impact factor: 4.132

5.  A case of partial mole and atypical type I triploidy associated with severe HELLP syndrome at 18 weeks' gestation.

Authors:  T Stefos; N Plachouras; G Mari; E Cosmi; D Lolis
Journal:  Ultrasound Obstet Gynecol       Date:  2002-10       Impact factor: 7.299

6.  Risk of preeclampsia in second-trimester triploid pregnancies.

Authors:  A Rijhsinghani; J Yankowitz; R A Strauss; J A Kuller; S Patil; R A Williamson
Journal:  Obstet Gynecol       Date:  1997-12       Impact factor: 7.661

7.  Prenatal diagnosis of triploidy during the second trimester of pregnancy.

Authors:  E Jauniaux; R Brown; C Rodeck; K H Nicolaides
Journal:  Obstet Gynecol       Date:  1996-12       Impact factor: 7.661

8.  Transient early preeclampsia in twin pregnancy with a triploid fetus: a case report.

Authors:  Clasien van der Houwen; Tineke Schukken; Mariëlle van Pampus
Journal:  J Med Case Rep       Date:  2009-05-26
  8 in total
  1 in total

1.  Maternal complications in molecularly confirmed diandric and digynic triploid pregnancies: single institution experience and literature review.

Authors:  D Massalska; J Bijok; A Kucińska-Chahwan; J G Zimowski; K Ozdarska; A Raniszewska; G M Panek; T Roszkowski
Journal:  Arch Gynecol Obstet       Date:  2020-03-26       Impact factor: 2.344

  1 in total

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