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Article

A familial case of recurrent hydatidiform mole with p.Asp108Ilefs∗30 causing mutation in KHDC3L: A genetic and clinical report.

Taiwanese journal of obstetrics & gynecology - 1 Mar 2022

Fatemi Nayeralsadat, Varkiani Maryam, Ramazanali Fariba, Almadani Navid, Totonchi Mehdi

Abstract excerpt

OBJECTIVE: Hydatidiform mole (HM) is defined by trophoblastic proliferation and vesicular enlargement of placental villi in which, KHDC3L gene plays a causal role. CASE REPORT: This report presents a clinical review and genetic screening for p.Asp108Ilefs∗30 mutation in KHDC3L gene in an affected woman with a previous history of HM and three siblings with a history of HM. Pathological examination of molar...

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Identifiers

PMID: 35361411
DOI: 10.1016/j.tjog.2022.02.038

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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