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Live births in women with recurrent hydatidiform mole and two NLRP7 mutations.
Akoury, Elie; Gupta, Neerja; Bagga, Rashmi; Brown, Stephen; Déry, Christine; Kabra, Madhulika; Srinivasan, Radhika; Slim, Rima.
Affiliation
  • Akoury E; Department of Human Genetics, McGill University Health Centre Research Institute, Glen Site, Montreal H4A 3J1, Canada; Department of Obstetrics and Gynecology, McGill University Health Centre Research Institute, Glen Site, Montreal H4A 3J1, Canada.
  • Gupta N; Genetic Unit, Department of Pediatrics, All India Institute of Medical Sciences in New Delhi (AIIMS), New Delhi, 110029, India.
  • Bagga R; Department of Obstetrics and Gynecology, Post Graduate Institute of Medical Education and Research, PGIMER, Chandigarh 160012, India.
  • Brown S; Department of Obstetrics and Gynecology, University of Vermont, Given 263, 89 Beaumont Ave., Burlington, VT 05405, USA.
  • Déry C; Department of Human Genetics, McGill University Health Centre Research Institute, Glen Site, Montreal H4A 3J1, Canada; Department of Obstetrics and Gynecology, McGill University Health Centre Research Institute, Glen Site, Montreal H4A 3J1, Canada.
  • Kabra M; Genetic Unit, Department of Pediatrics, All India Institute of Medical Sciences in New Delhi (AIIMS), New Delhi, 110029, India.
  • Srinivasan R; Cytology and Gynecological Pathology, Post Graduate Institute of Medical Education and Research, PGIMER, Chandigarh 160012, India.
  • Slim R; Department of Human Genetics, McGill University Health Centre Research Institute, Glen Site, Montreal H4A 3J1, Canada; Department of Obstetrics and Gynecology, McGill University Health Centre Research Institute, Glen Site, Montreal H4A 3J1, Canada. Electronic address: rima.slim@muhc.mcgill.ca.
Reprod Biomed Online ; 31(1): 120-4, 2015 Jul.
Article in En | MEDLINE | ID: mdl-25982095
Hydatidiform mole (HM) is an aberrant human pregnancy with abnormal embryonic development and excessive proliferation of the trophoblast. Recessive mutations in NLRP7 are responsible for recurrent HM (RHM). Women with recessive NLRP7 mutations fail to have normal pregnancies from spontaneous conceptions with the exception of three out of 131 reported patients. Because there is no treatment for RHM and maternal-effect genes are needed in the oocytes to sustain normal embryonic development until the activation of the embryonic genome, one patient with recessive NLRP7 mutations tried ovum donation and achieved a successful pregnancy. This study reports three additional live births from donated ova to two patients with recessive NLRP7 mutations. The occurrence of two live births from spontaneous conceptions to two other patients is also reported. The reproductive outcomes and mutations of all reported patients were reviewed and it was found that live births are associated with some missense mutations expected to have mild functional consequences on the protein. The data support a previous observation that ovum donation appears the best management option for these patients to achieve normal pregnancies and provide an explanation for the rare occurrence of live births from natural spontaneous conceptions in patients with two NLRP7 mutations.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pregnancy Outcome / Hydatidiform Mole / Live Birth / Infertility, Female Limits: Adult / Female / Humans / Pregnancy Language: En Journal: Reprod Biomed Online Journal subject: MEDICINA REPRODUTIVA Year: 2015 Document type: Article Affiliation country: Canadá Country of publication: Países Bajos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pregnancy Outcome / Hydatidiform Mole / Live Birth / Infertility, Female Limits: Adult / Female / Humans / Pregnancy Language: En Journal: Reprod Biomed Online Journal subject: MEDICINA REPRODUTIVA Year: 2015 Document type: Article Affiliation country: Canadá Country of publication: Países Bajos