Variants of NLRP genes encoding subcortical maternal complex components are linked to biparental placental mesenchymal dysplasia

Abstract Background Placental mesenchymal dysplasia (PMD) is a placental abnormality resembling partial hydatidiform moles without trophoblastic proliferation. Although many PMD cases involve androgenetic/biparental mosaicism or chimerism, we recently reported that approximately 30% of cases retain...

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Hlavní autoři:	Ayaka Murase, Hiroyuki Mishima, Saori Aoki, Satoshi Hara, Musashi Kubiura-Ichimaru, Takashi Ohba, Koh-ichiro Yoshiura, Hidenobu Soejima
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	BMC 2025-08-01
Edice:	Human Genomics
Témata:	Placental mesenchymal dysplasia Genomic imprinting Differentially methylated regions DNA methylation Subcortical maternal complex Multilocus imprinting disturbances
On-line přístup:	https://doi.org/10.1186/s40246-025-00814-w
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