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Gentagne diploid biparental molae

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Butt, Sedrah Arif et al. "Gentagne diploid biparental molae". Ugeskrift for Laeger. 2019, 181(33). V02190144.

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Bibtex

@article{c2985ad5bba846f78358218c4fb3bf48,
title = "Gentagne diploid biparental molae",
abstract = "This review summarises the knowledge of recurrent diploid biparental hydatidiform mole, which is a rare genetic condition. Pathogenic variants in both alleles of NLRP7 or KHDC3L are associated with maternal imprinting defects and can cause the condition. Women with biallelic inactivation of NLRP7 can achieve a normal pregnancy by oocyte donation, and it is highly likely, that this applies to women with biallelic inactivation of KHDCL3 as well. Identifying the cause of the recurrent moles can prevent that couples waist time and possibly reduce medical expenses related to fertility treatment.",
author = "Butt, {Sedrah Arif} and Louise Kelstrup and Marianne Lidang and Mette Bertelsen and Karen Ejrn{\ae}s and Lone Sunde and Perin, {Trine Lunde}",
year = "2019",
month = "8",
day = "12",
language = "Dansk",
volume = "181",
pages = "V02190144",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "33",

}

RIS

TY - JOUR

T1 - Gentagne diploid biparental molae

AU - Butt, Sedrah Arif

AU - Kelstrup, Louise

AU - Lidang, Marianne

AU - Bertelsen, Mette

AU - Ejrnæs, Karen

AU - Sunde, Lone

AU - Perin, Trine Lunde

PY - 2019/8/12

Y1 - 2019/8/12

N2 - This review summarises the knowledge of recurrent diploid biparental hydatidiform mole, which is a rare genetic condition. Pathogenic variants in both alleles of NLRP7 or KHDC3L are associated with maternal imprinting defects and can cause the condition. Women with biallelic inactivation of NLRP7 can achieve a normal pregnancy by oocyte donation, and it is highly likely, that this applies to women with biallelic inactivation of KHDCL3 as well. Identifying the cause of the recurrent moles can prevent that couples waist time and possibly reduce medical expenses related to fertility treatment.

AB - This review summarises the knowledge of recurrent diploid biparental hydatidiform mole, which is a rare genetic condition. Pathogenic variants in both alleles of NLRP7 or KHDC3L are associated with maternal imprinting defects and can cause the condition. Women with biallelic inactivation of NLRP7 can achieve a normal pregnancy by oocyte donation, and it is highly likely, that this applies to women with biallelic inactivation of KHDCL3 as well. Identifying the cause of the recurrent moles can prevent that couples waist time and possibly reduce medical expenses related to fertility treatment.

M3 - Tidsskriftartikel

VL - 181

SP - V02190144

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

SN - 0041-5782

IS - 33

ER -

ID: 58250707