1. Premature ovarian failure and fragile X premutation: a study on 45 women.
- Author
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Bussani C, Papi L, Sestini R, Baldinotti F, Bucciantini S, Bruni V, and Scarselli G
- Subjects
- Adult, Age Distribution, Blotting, Southern, Case-Control Studies, DNA Mutational Analysis, Female, Fragile X Syndrome diagnosis, Humans, Incidence, Italy epidemiology, Menopause, Premature genetics, Middle Aged, Primary Ovarian Insufficiency diagnosis, Primary Ovarian Insufficiency epidemiology, Reference Values, Risk Assessment, Sensitivity and Specificity, Chromosomes, Human, X genetics, Fragile X Syndrome genetics, Genetic Predisposition to Disease, Mutation, Primary Ovarian Insufficiency genetics
- Abstract
Objective: The aim of this study was to test for the presence of the fragile X (FRAXA) premutation a group of women with early menopause., Study Design: 45 women with idiopathic premature ovarian failure (POF), five with a familial and 40 with a sporadic form, were screened for the presence of FRAXA premutation. A control group of 28 women >45 years, with one or more children and no signs of POF, was also studied., Results: We found three cases of fragile X premutations in women all belonging to the group with sporadic POF., Conclusion: Our results seems to confirm previous observations on the non random association between POF and FRAXA premutation.
- Published
- 2004
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