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Recent insights on the genetics and epigenetics of endometriosis.
Borghese, B; Zondervan, K T; Abrao, M S; Chapron, C; Vaiman, D.
Afiliação
  • Borghese B; Cochin Institute, U1016 INSERM, CNRS 8104, Université Paris Descartes, Paris, France.
  • Zondervan KT; Department of Gynecology Obstetrics II and Reproductive Medicine, Faculté de Médecine, AP-HP, Groupe Hospitalier Ouest, Centre Hospitalier Universitaire Paris Centre, Paris, France.
  • Abrao MS; Nuffield Department of Obstetrics and Gynaecology, Endometriosis Care Centre, University of Oxford, Oxford, UK.
  • Chapron C; Endometriosis Division, Obstetrics and Gynecology Department, Sao Paulo University, Sao Paulo, Brazil.
  • Vaiman D; Reproductive Clinic, Sirio Libanes Hospital, Sao Paulo, Brazil.
Clin Genet ; 91(2): 254-264, 2017 02.
Article em En | MEDLINE | ID: mdl-27753067
Endometriosis is a gynecologic disease affecting up to 10% of the women and a major cause of pain and infertility. It is characterized by the implantation of functional endometrial tissue at ectopic positions generally within the peritoneum. This complex disease has an important genetic component with a heritability estimated at around 50%. This review aims at providing recent insights into the genetic bases of endometriosis, and presents a detailed overview of evidence of epigenetic alterations specific to this disease. In the future, these alterations may constitute therapeutic targets for pharmacological compounds able to modify the epigenetic code.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epigênese Genética / Endometriose / Infertilidade Feminina Limite: Female / Humans Idioma: En Revista: Clin Genet Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epigênese Genética / Endometriose / Infertilidade Feminina Limite: Female / Humans Idioma: En Revista: Clin Genet Ano de publicação: 2017 Tipo de documento: Article