Literature DB >> 21439709

The spectrum of NLRP7 mutations in French patients with recurrent hydatidiform mole.

Joël Muhlstein1, François Golfier, Cécile Rittore, Touria Hajri, Laurent Philibert, Fabienne Abel, Claire Beneteau, Isabelle Touitou.   

Abstract

OBJECTIVES: The NLRP7 gene (19q13.42) is associated with recurrent and/or familial hydatidiform moles. Several mutations, histopathological types and reproductive outcomes have been described. We studied our recurrent hydatidiform mole cases recorded since 1999 in order to identify links between clinic, histology and genetics. STUDY: We present here the gestational history and the spectrum of NLRP7 mutations in our French series.
DESIGN: We performed a retrospective study from clinical forms received for genetic diagnosis. Cases declaration was based on a voluntary initiative coming from French practitioners, subjected to patients' agreement.
RESULTS: Among 12 recurrent hydatidiform moles investigated, we identified 3 cases of confirmed homozygous NLRP7 mutation and 3 cases of heterozygous NLRP7 mutation. One patient bore a novel mutation p.Leu880Ser in a homozygous state.
CONCLUSIONS: We here identified a new homozygous NLRP7 mutation. Unfortunately, no modern therapeutic option has proven effective to obtain evolutive pregnancies. Then, fundamental and clinical researches seem to be necessary. Moreover, collecting RHM cases is essential.
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.

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Year:  2011        PMID: 21439709     DOI: 10.1016/j.ejogrb.2011.02.019

Source DB:  PubMed          Journal:  Eur J Obstet Gynecol Reprod Biol        ISSN: 0301-2115            Impact factor:   2.435


  5 in total

1.  Pregnancy after oocyte donation in a patient with NLRP7 gene mutations and recurrent molar hydatidiform pregnancies.

Authors:  Claire Cozette; Florence Scheffler; Melyne Lombart; Jerome Massardier; Pierre-Adrien Bolze; Touria Hajri; Francois Golfier; Isabelle Touitou; Cecile Rittore; Jean Gondry; Philippe Merviel; Moncef Benkhalifa; Rosalie Cabry
Journal:  J Assist Reprod Genet       Date:  2020-06-26       Impact factor: 3.412

2.  Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.

Authors:  David A Parry; Clare V Logan; Bruce E Hayward; Michael Shires; Hanène Landolsi; Christine Diggle; Ian Carr; Cécile Rittore; Isabelle Touitou; Laurent Philibert; Rosemary A Fisher; Masoumeh Fallahian; John D Huntriss; Helen M Picton; Saghira Malik; Graham R Taylor; Colin A Johnson; David T Bonthron; Eamonn G Sheridan
Journal:  Am J Hum Genet       Date:  2011-09-01       Impact factor: 11.025

3.  No evidence for mutations in NLRP7, NLRP2 or KHDC3L in women with unexplained recurrent pregnancy loss or infertility.

Authors:  L Aghajanova; S Mahadevan; S Altmäe; A Stavreus-Evers; L Regan; N Sebire; P Dixon; R A Fisher; I B Van den Veyver
Journal:  Hum Reprod       Date:  2014-11-05       Impact factor: 6.918

4.  NLRP7, a nucleotide oligomerization domain-like receptor protein, is required for normal cytokine secretion and co-localizes with Golgi and the microtubule-organizing center.

Authors:  Christiane Messaed; Elie Akoury; Ugljesa Djuric; Jibin Zeng; Maya Saleh; Lucy Gilbert; Muhieddine Seoud; Salman Qureshi; Rima Slim
Journal:  J Biol Chem       Date:  2011-10-24       Impact factor: 5.157

5.  Variable Number Tandem Repeat (VNTR) Genotyping of Hydatidiform Mole in Iranian Patients.

Authors:  Zahra Pakzad; Hossein Mozdarani; Narges Izadi-Mood; Shirin Niromanesh
Journal:  Avicenna J Med Biotechnol       Date:  2014-10
  5 in total

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