Mutations in NLRP7 are associated with diploid biparental hydatidiform moles, but not androgenetic complete moles

NLRP7 (NALP7) has been identified as the major gene involved in the inherited predisposition to recurrent molar pregnancies, a rare recessive condition in which affected individuals have complete hydatidiform moles of diploid biparental origin (BiCHM). The role of NLRP7 in other types of molar pregn...

Full description

Saved in:

Bibliographic Details
Published in:	Journal of medical genetics Vol. 49; no. 3; p. 206
Main Authors:	Dixon, Peter H, Trongwongsa, Pirada, Abu-Hayyah, Shadi, Ng, Sze Hwei, Akbar, Syed Ali, Khawaja, Nuzhat P, Seckl, Michael J, Savage, Philip M, Fisher, Rosemary A
Format:	Journal Article
Language:	English
Published:	England 01-03-2012
Subjects:	Adaptor Proteins, Signal Transducing - genetics Case-Control Studies Diploidy DNA Mutational Analysis Female Genetic Association Studies Humans Hydatidiform Mole - genetics Mutation, Missense Neoplasm Recurrence, Local - genetics Polymorphism, Single Nucleotide Pregnancy
Online Access:	Get more information
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Summary:	NLRP7 (NALP7) has been identified as the major gene involved in the inherited predisposition to recurrent molar pregnancies, a rare recessive condition in which affected individuals have complete hydatidiform moles of diploid biparental origin (BiCHM). The role of NLRP7 in other types of molar pregnancy and reproductive wastage has not been conclusively demonstrated. The purpose of this study was to clarify this by identifying NLRP7 variation in two clinically well-defined groups of patients: women with recurrent BiCHM, and women with three or more recurrent complete hydatidiform moles of proven androgenetic origin (AnCHM). Fluorescent microsatellite genotyping of molar tissue was used to establish a diagnosis of recurrent BiCHM (four novel cases) or recurrent AnCHM (nine women with multiple CHM). These two groups were subsequently screened for mutations in NLRP7 using DNA sequencing. Additional screening for non-pathological variants was performed in 21 previously published cases of recurrent BiCHM. Taqman genotyping was used to determine the frequency of novel NLRP7 variants in two control cohorts of Caucasian and Asian women with no adverse reproductive outcomes. Of the four novel cases with recurrent BiCHM, two were homozygous for mutations in NLRP7 while one was a compound heterozygote for a nonsense mutation and a pathological variant. No NLRP7 mutations or pathological variants were identified in the fourth case. None of the women with AnCHM carried any mutations or pathological variants of NLRP7. A single case of AnCHM was found to be heterozygous for a novel variant (R413Q). NLRP7 mutations do not represent a major cause of AnCHM.
ISSN:	1468-6244
DOI:	10.1136/jmedgenet-2011-100602