Endometriose und Adenomyose
Endometriosis is a complex disease where genetic alterations and altered gene expression patterns are implicated in its pathogenesis and heredity.
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The paper discusses endometriosis as a highly complex disease and examines the plausibility of hereditary influences based on observations of familial clustering and sibling occurrence. It reports that larger studies can appear to support heredity, and that altered gene expression patterns have been used to better understand disease pathomechanisms, while genome-wide association studies have identified genomic “hotspots” related to inheritance. The authors explicitly note that clear, indisputable evidence for a definitive hereditary pattern is still lacking, which is a key limitation of the overall argument. This paper is centrally about endometriosis — it focuses on heredity, gene expression alterations, and genome-wide association findings as components of endometriosis pathogenetic understanding.
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References (11)
- Defective myometrial spiral artery remodelling as a cause of major obstetrical syndromes in endometriosis and adenomyosis via openalex
- Endometriosis via openalex
- Genetic burden associated with varying degrees of disease severity in endometriosis via openalex
- Heritability of endometriosis via openalex
- Heritable aspects of endometriosis via openalex
- Promoter Methylation Regulates Estrogen Receptor 2 in Human Endometrium and Endometriosis1 via openalex
- W2151934245 via openalex
- W2152628855 via openalex
- W2507981487 via openalex
- W2617005810 via openalex
- W2123971761 via openalex
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