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Outcome of Subsequent Pregnancies in Familial Molar Pregnancy
Familial recurrent molar pregnancy is an exceedingly rare condition, in which complete hydatidiform moles are mostly diploid but biparental in origin and the outcome of subsequent pregnancies is likely to be a hydatidiform mole or other type of reproductive loss. We previously reported a case of fam...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royan Institute
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850334/ https://www.ncbi.nlm.nih.gov/pubmed/24520466 |
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author | Fallahian, Masoumeh Foroughi, Forough Vasei, Mohammad Tavana, Shahrzad Ghanbary, Maryam Monajemzadeh, Maryam Tavana, Anahita |
author_facet | Fallahian, Masoumeh Foroughi, Forough Vasei, Mohammad Tavana, Shahrzad Ghanbary, Maryam Monajemzadeh, Maryam Tavana, Anahita |
author_sort | Fallahian, Masoumeh |
collection | PubMed |
description | Familial recurrent molar pregnancy is an exceedingly rare condition, in which complete hydatidiform moles are mostly diploid but biparental in origin and the outcome of subsequent pregnancies is likely to be a hydatidiform mole or other type of reproductive loss. We previously reported a case of familial molar pregnancy (family K) comprising five affected members (four sisters and one of their cousins) each with at least one hydatidiform mole (HM). In addition to the molar pregnancies, these patients have a total of three miscarriages and 8 normal pregnancies leading to healthy children; but the youngest member of this family has given birth to a boy with Down syndrome. Our second family (case S) includes two sisters with diploid biparental complete moles. They have a total of six molar pregnancies with no living child. Recently the younger sister had a partial molar pregnancy with apparently normal XX fetus accompanying diffuse molar changes of the placenta that led to preeclampsia and preterm delivery. Overall, these families have had 26 pregnancies including 12 molar pregnancies (complete or partial) and three abortions. We concluded that these families are predisposed to various genetic mutations, chromosomal abnormalities and clinical manifestations, which affect their offspring. Further studies of patients are needed to determine any relationship between a history of familial molar pregnancy and trisomy or other chromosomal abnormalities in offspring and genetic mutations in the products of conception to complete the puzzle and manage familial molar pregnancy. |
format | Online Article Text |
id | pubmed-3850334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-38503342014-02-11 Outcome of Subsequent Pregnancies in Familial Molar Pregnancy Fallahian, Masoumeh Foroughi, Forough Vasei, Mohammad Tavana, Shahrzad Ghanbary, Maryam Monajemzadeh, Maryam Tavana, Anahita Int J Fertil Steril Case Report Familial recurrent molar pregnancy is an exceedingly rare condition, in which complete hydatidiform moles are mostly diploid but biparental in origin and the outcome of subsequent pregnancies is likely to be a hydatidiform mole or other type of reproductive loss. We previously reported a case of familial molar pregnancy (family K) comprising five affected members (four sisters and one of their cousins) each with at least one hydatidiform mole (HM). In addition to the molar pregnancies, these patients have a total of three miscarriages and 8 normal pregnancies leading to healthy children; but the youngest member of this family has given birth to a boy with Down syndrome. Our second family (case S) includes two sisters with diploid biparental complete moles. They have a total of six molar pregnancies with no living child. Recently the younger sister had a partial molar pregnancy with apparently normal XX fetus accompanying diffuse molar changes of the placenta that led to preeclampsia and preterm delivery. Overall, these families have had 26 pregnancies including 12 molar pregnancies (complete or partial) and three abortions. We concluded that these families are predisposed to various genetic mutations, chromosomal abnormalities and clinical manifestations, which affect their offspring. Further studies of patients are needed to determine any relationship between a history of familial molar pregnancy and trisomy or other chromosomal abnormalities in offspring and genetic mutations in the products of conception to complete the puzzle and manage familial molar pregnancy. Royan Institute 2013 2013-03-06 /pmc/articles/PMC3850334/ /pubmed/24520466 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Fallahian, Masoumeh Foroughi, Forough Vasei, Mohammad Tavana, Shahrzad Ghanbary, Maryam Monajemzadeh, Maryam Tavana, Anahita Outcome of Subsequent Pregnancies in Familial Molar Pregnancy |
title | Outcome of Subsequent Pregnancies in Familial Molar
Pregnancy |
title_full | Outcome of Subsequent Pregnancies in Familial Molar
Pregnancy |
title_fullStr | Outcome of Subsequent Pregnancies in Familial Molar
Pregnancy |
title_full_unstemmed | Outcome of Subsequent Pregnancies in Familial Molar
Pregnancy |
title_short | Outcome of Subsequent Pregnancies in Familial Molar
Pregnancy |
title_sort | outcome of subsequent pregnancies in familial molar
pregnancy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850334/ https://www.ncbi.nlm.nih.gov/pubmed/24520466 |
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