Literature DB >> 29436108

A fetus coexisting with a complete hydatidiform mole with trisomy 9 of maternal origin.

Anita Sik Yau Kan1, Elizabeth Tak Kwong Lau2, Chun Hong So3, Wan Pang Chan3, Wing Cheuk Wong4, Kam Cheong Lee4, Mark D Pertile5,6, Mary Hoi Yin Tang2.   

Abstract

A complete hydatidiform mole (CHM) coexisting with a viable fetus is a rare finding in pregnancies. Accurate diagnosis often relies on ultrasonographic, histopathological and molecular techniques in the definite diagnosis. To the best of our knowledge, a liveborn fetus coexisting with CHM with trisomy 9 has not been described. The use of molecular genotyping and immunohistochemical laboratory investigations enabled the CHM to be fully characterized. Postzygotic diploidization of a triploid conception arising from dispermy is the proposed mechanism of its formation.
© 2018 Japan Society of Obstetrics and Gynecology.

Entities:  

Keywords:  cytogenetics; multiple gestation; obstetrics: diagnostic ultrasound and prenatal diagnosis; placental pathology

Mesh:

Year:  2018        PMID: 29436108     DOI: 10.1111/jog.13598

Source DB:  PubMed          Journal:  J Obstet Gynaecol Res        ISSN: 1341-8076            Impact factor:   1.730


  2 in total

1.  Genome-wide single nucleotide polymorphism array analysis unveils the origin of heterozygous androgenetic complete moles.

Authors:  Hirokazu Usui; Kazuhiko Nakabayashi; Kayoko Maehara; Kenichiro Hata; Makio Shozu
Journal:  Sci Rep       Date:  2019-08-29       Impact factor: 4.379

2.  Parental contribution to trisomy in heterozygous androgenetic complete moles.

Authors:  Hirokazu Usui; Asuka Sato; Makio Shozu
Journal:  Sci Rep       Date:  2020-10-13       Impact factor: 4.379

  2 in total

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