Familial Recurrent Hydatidiform Moles: A rare case report

Cilt: 1 Sayı: 3 1 Eylül 2014
  • Fatma Eskicioglu
  • Isin Kaya
  • Esra Bahar Gur
  • Guluzar Arzu Turan
Medical Science and Discovery Kapak
Medical Science and Discovery
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Familial Recurrent Hydatidiform Moles: A rare case report

Abstract

Recurrent hydatidiform moles (RHM) are described as the being of at least two molar pregnancies in the same patient. It is very rare. NLPR7 mutations are found high rate in patients with RHM. KHDC3L is the second responsible gene for RHM. In this paper, we present an interesting case of a familial RHM. Here, we have discussed the genetic counseling to be given to a patient who had been diagnosed as hydatidiform mole in her two previous pregnancies and whose sister had a history of four consecutive molar pregnancies. Because rate of NLPR7 mutation is high in individuals with recurrent molar pregnancy, patients should be recommended to have NLRP7 gene sequence analysis in the first place. If no mutation is detected in this gene, KHDC3l gene sequence analysis should be carried out

Keywords

Kaynakça

  1. Copyright © 2014 The Author(s); This is an open-access article distributed under the terms of the Creative Commons Attribution
  2. License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium,
  3. provided the original work is properly cited.

Ayrıntılar

Birincil Dil

İngilizce

Konular

-

Bölüm

-

Yazarlar

Fatma Eskicioglu Bu kişi benim

Esra Bahar Gur Bu kişi benim

Guluzar Arzu Turan Bu kişi benim

Yayımlanma Tarihi

1 Eylül 2014

Gönderilme Tarihi

26 Aralık 2014

Kabul Tarihi

-

Yayımlandığı Sayı

Yıl 2014 Cilt: 1 Sayı: 3

DOI

https://doi.org/10.17546/msd.80072

IZ

https://izlik.org/JA88HU44DJ

Kaynak Göster

RIS / Bibtex
APA
Eskicioglu, F., Kaya, I., Gur, E. B., & Turan, G. A. (2014). Familial Recurrent Hydatidiform Moles: A rare case report. Medical Science and Discovery, 1(3), 85-87. https://doi.org/10.17546/msd.80072
AMA
1.Eskicioglu F, Kaya I, Gur EB, Turan GA. Familial Recurrent Hydatidiform Moles: A rare case report. Med Sci Discov. 2014;1(3):85-87. doi:10.17546/msd.80072
Chicago
Eskicioglu, Fatma, Isin Kaya, Esra Bahar Gur, ve Guluzar Arzu Turan. 2014. “Familial Recurrent Hydatidiform Moles: A rare case report”. Medical Science and Discovery 1 (3): 85-87. https://doi.org/10.17546/msd.80072.
EndNote
Eskicioglu F, Kaya I, Gur EB, Turan GA (01 Eylül 2014) Familial Recurrent Hydatidiform Moles: A rare case report. Medical Science and Discovery 1 3 85–87.
IEEE
[1]F. Eskicioglu, I. Kaya, E. B. Gur, ve G. A. Turan, “Familial Recurrent Hydatidiform Moles: A rare case report”, Med Sci Discov, c. 1, sy 3, ss. 85–87, Eyl. 2014, doi: 10.17546/msd.80072.
ISNAD
Eskicioglu, Fatma - Kaya, Isin - Gur, Esra Bahar - Turan, Guluzar Arzu. “Familial Recurrent Hydatidiform Moles: A rare case report”. Medical Science and Discovery 1/3 (01 Eylül 2014): 85-87. https://doi.org/10.17546/msd.80072.
JAMA
1.Eskicioglu F, Kaya I, Gur EB, Turan GA. Familial Recurrent Hydatidiform Moles: A rare case report. Med Sci Discov. 2014;1:85–87.
MLA
Eskicioglu, Fatma, vd. “Familial Recurrent Hydatidiform Moles: A rare case report”. Medical Science and Discovery, c. 1, sy 3, Eylül 2014, ss. 85-87, doi:10.17546/msd.80072.
Vancouver
1.Fatma Eskicioglu, Isin Kaya, Esra Bahar Gur, Guluzar Arzu Turan. Familial Recurrent Hydatidiform Moles: A rare case report. Med Sci Discov. 01 Eylül 2014;1(3):85-7. doi:10.17546/msd.80072