Müllerian anomalies and endometriosis: associations and phenotypic variations

dc.contributor.authorBhamidipaty-Pelosi, Surya
dc.contributor.authorKyei-Barffour, Isaac
dc.contributor.authorVolpert, Marianna
dc.contributor.authorO’Neill, Nora
dc.contributor.authorGrimshaw, Alyssa
dc.contributor.authorEriksson, Lars
dc.contributor.authorVash-Margita, Alla
dc.contributor.authorPelosi, Emanuele
dc.contributor.departmentBiochemistry and Molecular Biology, School of Medicine
dc.date.accessioned2025-01-24T11:40:49Z
dc.date.available2025-01-24T11:40:49Z
dc.date.issued2024-12-19
dc.description.abstractMüllerian anomalies are congenital conditions characterized by the incomplete development of the female reproductive tract. Women affected by Müllerian anomalies often display additional malformations of the renal, skeletal, and cardiovascular system, and are at a higher risk for infertility and adverse pregnancy outcomes. Several Müllerian anomalies have been reported in association with endometriosis, but it is unclear if all classes or anatomical variations are associated with the disease. Most importantly, both Müllerian anomalies and endometriosis can manifest with a wide degree of variability, adding further complexity to their poorly defined relationship. Retrograde menstruation occurring in obstructive Müllerian anomalies is a well-accepted mechanism for the development of endometriosis. However, endometriosis can occur following surgical correction of the anomaly or in the absence of obstruction. This suggests that other mechanisms may be involved, although the specific pathogenesis remains elusive. This review provides a comprehensive summary of the current state of clinical research on endometriosis in Müllerian anomalies. This review also highlights research and knowledge gaps, informing the development of future experimental designs to address current limitations including heterogeneity of phenotypes, variable comorbidities, and lack of genetic information.
dc.eprint.versionFinal published version
dc.identifier.citationBhamidipaty-Pelosi S, Kyei-Barffour I, Volpert M, et al. Müllerian anomalies and endometriosis: associations and phenotypic variations. Reprod Biol Endocrinol. 2024;22(1):157. Published 2024 Dec 19. doi:10.1186/s12958-024-01336-1
dc.identifier.urihttps://hdl.handle.net/1805/45450
dc.language.isoen_US
dc.publisherSpringer Nature
dc.relation.isversionof10.1186/s12958-024-01336-1
dc.relation.journalReproductive Biology and Endocrinology
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0
dc.sourcePMC
dc.subjectMRKH syndrome
dc.subjectMüllerian anomalies
dc.subjectBicornuate
dc.subjectDidelphys
dc.subjectEndometriosis
dc.subjectSeptate
dc.subjectUnicornuate
dc.titleMüllerian anomalies and endometriosis: associations and phenotypic variations
dc.typeArticle
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