Literature DB >> 20553678

Chromosomal anomaly spectrum in early pregnancy loss in relation to presence or absence of an embryonic pole.

Monica Muñoz1, Marta Arigita, Mar Bennasar, Anna Soler, Aurora Sanchez, Antoni Borrell.   

Abstract

OBJECTIVE: To compare the cytogenetic findings in a series of missed miscarriages evaluated by chorionic villus sampling, in relation to embryonic pole presence (embryonic or anembryonic).
DESIGN: Prospective cross-sectional study.
SETTING: Tertiary referral hospital. PATIENT(S): Women presenting with a missed miscarriage. INTERVENTION(S): Transcervical chorionic villus sampling and cytogenetic studies in the chorionic villi with use of the semidirect method. MAIN OUTCOME MEASURES(S): Embryonic pole presence or absence assessed by transvaginal ultrasound examination. Type of chromosomal anomalies found in both subgroups. RESULT(S): Although the chromosomal abnormality rate was similar for miscarriages with absent or present embryo (61% vs. 68% respectively), frequencies for viable autosomal trisomies (2.3% vs. 19%) and monosomy X (0% vs. 9.2%) were significantly lower when no embryonic pole was seen. CONCLUSION(S): Viable autosomal trisomies and monosomies X appear not to be a common cause of miscarriage with an early fetal demise (anembryonic miscarriage).
Copyright © 2010 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20553678     DOI: 10.1016/j.fertnstert.2010.04.011

Source DB:  PubMed          Journal:  Fertil Steril        ISSN: 0015-0282            Impact factor:   7.329


  9 in total

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2.  Chromosome distribution of early miscarriages with present or absent embryos: female predominance.

Authors:  Hsin-Hsin Cheng; Chia-Yu Ou; Ching-Chang Tsai; Shuenn-Dyh Chang; Pi-Yu Hsiao; Kuo-Chung Lan; Te-Yao Hsu
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3.  Maternal age, history of miscarriage, and embryonic/fetal size are associated with cytogenetic results of spontaneous early miscarriages.

Authors:  Nobuaki Ozawa; Kohei Ogawa; Aiko Sasaki; Mari Mitsui; Seiji Wada; Haruhiko Sago
Journal:  J Assist Reprod Genet       Date:  2019-02-09       Impact factor: 3.412

4.  Identification of Xq22.1-23 as a region linked with hereditary recurrent spontaneous abortion in a family.

Authors:  Sahar Shekouhi; Fatemeh Baghbani; Mohammad Hasanzadeh Nazar-Abadi; Tayebeh Hamzehloie; Mohammad Reza Abbaszadegan; Nafiseh Saghafi; Reza Raoofian; Javad Zavar Reza; Shahab Ahmadzadeh; Mohammad Amin Tabatabaiefar; Majid Mojarrad
Journal:  Iran J Reprod Med       Date:  2013-08

5.  Polymorphism of MnSOD (Val16Ala) gene in pregnancies with blighted ovum: A case-control study.

Authors:  Asiyeh Moshtaghi; Hamidreza Vaziri; Reyhaneh Sariri; Hoorieh Shaigan
Journal:  Int J Reprod Biomed (Yazd)       Date:  2017-08

6.  Whole‑exome sequencing analysis of products of conception identifies novel mutations associated with missed abortion.

Authors:  Meng Fu; Sha Mu; Chunyan Wen; Shufang Jiang; Lin Li; Yuanguang Meng; Hongmei Peng
Journal:  Mol Med Rep       Date:  2018-06-21       Impact factor: 2.952

7.  Do specific ultrasonography features identified at the time of early pregnancy loss predict fetal chromosomal abnormality? - A systematic review and meta-analysis.

Authors:  J Huang; W Zhu; J Tang; S H Saravelos; L C Y Poon; T C Li
Journal:  Genes Dis       Date:  2018-10-13

8.  Chromosomal Aneuploidy Associated With Clinical Characteristics of Pregnancy Loss.

Authors:  Chongjuan Gu; Kuanrong Li; Ru Li; Ling Li; Xiaojun Li; Xinyu Dai; Yaojuan He
Journal:  Front Genet       Date:  2021-04-15       Impact factor: 4.599

9.  Chromosomal study of couples with the history of recurrent spontaneous abortions with diagnosed blightded ovum.

Authors:  Sahar Shekoohi; Majid Mojarrad; Reza Raoofian; Shahab Ahmadzadeh; Salmah Mirzaie; Mohammad Hassanzadeh-Nazarabadi
Journal:  Int J Mol Cell Med       Date:  2013
  9 in total

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