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Utilizing FMR1 gene mutations as predictors of treatment success in human in vitro fertilization
- Source :
- PLoS ONE, Vol 9, Iss 7, p e102274 (2014), PLoS ONE
- Publication Year :
- 2014
- Publisher :
- Public Library of Science (PLoS), 2014.
-
Abstract
- CONTEXT Mutations of the fragile X mental retardation 1 (FMR1) gene are associated with distinct ovarian aging patterns. OBJECTIVE To confirm in human in vitro fertilization (IVF) that FMR1 affects outcomes, and to determine whether this reflects differences in ovarian aging between FMR1 mutations, egg/embryo quality or an effect on implantation. DESIGN, SETTING, PATIENTS IVF outcomes were investigated in a private infertility center in reference to patients' FMR1 mutations based on a normal range of CGG(n = 26-34) and sub-genotypes high (CGG(n>34)) and low (CGG(
- Subjects :
- Infertility
Genetic Markers
congenital, hereditary, and neonatal diseases and abnormalities
Pregnancy Rate
medicine.medical_treatment
Aneuploidy
lcsh:Medicine
Context (language use)
Fertilization in Vitro
Bioinformatics
Assisted Reproductive Technology
Andrology
Fragile X Mental Retardation Protein
Pregnancy
medicine
Medicine and Health Sciences
Odds Ratio
Humans
lcsh:Science
Multidisciplinary
In vitro fertilisation
business.industry
Female infertility
Ovary
lcsh:R
Obstetrics and Gynecology
medicine.disease
Embryo, Mammalian
FMR1
nervous system diseases
Treatment Outcome
Mutation
embryonic structures
Women's Health
Female
lcsh:Q
business
Embryo quality
Research Article
Subjects
Details
- Language :
- English
- ISSN :
- 19326203
- Volume :
- 9
- Issue :
- 7
- Database :
- OpenAIRE
- Journal :
- PLoS ONE
- Accession number :
- edsair.doi.dedup.....4468ff804ac4cfc41b9d250d9eabfa9d