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Article

A ZP1 gene mutation in a patient with empty follicle syndrome: A case report and literature review.

European journal of obstetrics, gynecology, and reproductive biology - 1 Jan 2023

Pujalte Mathilde, Camo Maïté, Celton Noémie, Attencourt Christophe, Lefranc Elodie, Jedraszak Guillaume, Scheffler Florence

Abstract excerpt

Genuine empty follicle syndrome (gEFS) is a rare cause of female infertility; it is defined as the presence of cumulus-oocyte complexes (COCs) in follicular fluid but the absence of oocytes after denudation in an in vitro fertilization (IVF) programme. Mutations in one of the four genes encoding zona pellucida (ZP) proteins have been implicated in gEFS. The objectives of the present study were to explore the...

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PMID: 36529558
DOI: 10.1016/j.ejogrb.2022.12.011

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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A ZP1 gene mutation in a patient with empty follicle syndrome: A case report and literature review.PMID 36529558Read ↗

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The critical role of ZP genes in female infertility characterized by empty follicle syndrome and oocyte degeneration.Semantic proximity Read ↗

A Novel Homozygous Nonsense Mutation in ZP1 Causes Female Infertility due to Empty Follicle Syndrome.Semantic proximity Read ↗

A Novel Homozygous Missense ZP1 Variant Result in Human Female Empty Follicle Syndrome.Semantic proximity Read ↗

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