PGD for fragile X syndrome: ovarian function is the main determinant of success
Author(s) -
Avi Tsafrir,
Gheona Altarescu,
Ehud J. Margalioth,
B. Brooks,
Paul Renbaum,
Ephrat LevyLahad,
Ron Rabinowitz,
Irit Varshaver,
Talia EldarGeva
Publication year - 2010
Publication title -
human reproduction
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.446
H-Index - 226
eISSN - 1460-2350
pISSN - 0268-1161
DOI - 10.1093/humrep/deq203
Subject(s) - medicine , embryo transfer , frax , gynecology , fragile x syndrome , pregnancy rate , obstetrics , pregnancy , fragile x , andrology , biology , genetics , gene , bone mineral , osteoporosis , osteoporotic fracture , psychiatry
PGD for fragile X syndrome (FRAX) is inefficient, probably owing to fewer oocytes, poor embryo quality and difficulties in genetic analysis. We investigated IVF-PGD in FRAX mutation carriers compared with controls, looking at the effects of oocyte and embryo number/quality on live birth outcome.
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