Skip Navigation

This Article
Right arrow FREE Full Text (PDF ) Freely available
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (50)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Vegetti, W.
Right arrow Articles by Crosignani, P. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vegetti, W.
Right arrow Articles by Crosignani, P. G.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Reproduction, Vol 13, 1796-1800, Copyright © 1998 by Oxford University Press


ARTICLES

Inheritance in idiopathic premature ovarian failure: analysis of 71 cases

W Vegetti, M Grazia Tibiletti, G Testa, Yankowski de Lauretis, F Alagna, E Castoldi, M Taborelli, T Motta, PF Bolis, L Dalpra and PG Crosignani
First Department of Obstetrics and Gynaecology, University of Milan, Italy.

Premature ovarian failure is defined as cessation of ovarian function under the age of 40 years and affects approximately 1% of women in the general population. The aetiology of this disorder is still unknown in most cases. Although there have been some reports of familial premature ovarian failure, very little is known about the incidence and inheritance pattern of its idiopathic form. The aims of this study were to investigate the incidence and inheritance pattern of familial premature ovarian failure in a homogeneous group of patients with premature idiopathic menopause and to identify possible clinical differences between patients with the familial and the sporadic form of premature ovarian failure. A total of 71 women were recruited into the study. Clinical assessments and genetic counselling showed that 22 (31%) patients had familial premature ovarian failure, this high incidence strongly suggesting that the disorder is a recognizable heritable entity. There was a statistically significant (P < 0.05) difference in the median age of precocious menopause in patients with sporadic and familial premature ovarian failure (31.0 and 37.5 years of age in the two groups, respectively). Pedigree analysis strongly suggests the existence of a familial pattern of premature ovarian failure with a dominant maternal and/or paternal transmission and incomplete penetrance. In the presence of familial history of premature ovarian failure, reproductive counselling is recommended.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mol Hum ReprodHome page
E. Zintzaras
Inhibin alpha gene and susceptibility to premature ovarian failure: a data synthesis
Mol. Hum. Reprod., September 1, 2009; 15(9): 551 - 555.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
B. Wang, L. Li, F. Ni, J. Song, J. Wang, Y. Mu, X. Ma, and Y. Cao
Mutational analysis of SAL-Like 4 (SALL4) in Han Chinese women with premature ovarian failure
Mol. Hum. Reprod., September 1, 2009; 15(9): 557 - 562.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
R.A. Oldenburg, M.F. van Dooren, B. de Graaf, E. Simons, L. Govaerts, S. Swagemakers, J.M.H. Verkerk, B.A. Oostra, and A.M. Bertoli-Avella
A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus
Hum. Reprod., December 1, 2008; 23(12): 2835 - 2841.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
A. L. Chand, G. T. Ooi, C. A. Harrison, A. N. Shelling, and D. M. Robertson
Functional analysis of the human inhibin {alpha} subunit variant A257T and its potential role in premature ovarian failure
Hum. Reprod., December 1, 2007; 22(12): 3241 - 3248.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
F. Rizzolio, S. Bione, C. Sala, M. Goegan, M. Gentile, G. Gregato, E. Rossi, T. Pramparo, O. Zuffardi, and D. Toniolo
Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literature
Hum. Reprod., June 1, 2006; 21(6): 1477 - 1483.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
W. J. Watkins, S. E. Harris, M. J. Craven, A. L. Vincent, I. M. Winship, K. Gersak, and A. N. Shelling
An investigation into FOXE1 polyalanine tract length in premature ovarian failure
Mol. Hum. Reprod., March 1, 2006; 12(3): 145 - 149.
[Abstract] [Full Text] [PDF]


Home page
Hum Reprod UpdateHome page
D. Goswami and G. S. Conway
Premature ovarian failure
Hum. Reprod. Update, July 1, 2005; 11(4): 391 - 410.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
B. Bodega, C. Porta, P.G. Crosignani, E. Ginelli, and A. Marozzi
Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure
Mol. Hum. Reprod., August 1, 2004; 10(8): 555 - 557.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
S.E. Harris, A.L. Chand, I.M. Winship, K. Gersak, K. Aittomaki, and A.N. Shelling
Identification of novel mutations in FOXL2 associated with premature ovarian failure
Mol. Hum. Reprod., August 1, 2002; 8(8): 729 - 733.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
A. Marozzi, C. Porta, W. Vegetti, P.G. Crosignani, M.G. Tibiletti, L. Dalpra, and E. Ginelli
Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failure
Hum. Reprod., July 1, 2002; 17(7): 1741 - 1745.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
A. N. Shelling, K. A. Burton, A. L. Chand, C. C. van Ee, J. T. France, C. M. Farquhar, S. R. Milsom, D. R. Love, K. Gersak, K. Aittomaki, et al.
Inhibin: a candidate gene for premature ovarian failure
Hum. Reprod., December 1, 2000; 15(12): 2644 - 2649.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
C. J. Davis, R. M. Davison, N. N. Payne, C. H. Rodeck, and G. S. Conway
Female sex preponderance for idiopathic familial premature ovarian failure suggests an X chromosome defect: Opinion
Hum. Reprod., November 1, 2000; 15(11): 2418 - 2422.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
A. Marozzi, W. Vegetti, E. Manfredini, M. G. Tibiletti, G. Testa, P. G. Crosignani, E. Ginelli, R. Meneveri, and L. Dalpra
Association between idiopathic premature ovarian failure and fragile X premutation
Hum. Reprod., January 1, 2000; 15(1): 197 - 202.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
M.G. Tibiletti, G. Testa, W. Vegetti, F. Alagna, M. Taborelli, L. Dalpra, P.F. Bolis, and P.G. Crosignani
The idiopathic forms of premature menopause and early menopause show the same genetic pattern
Hum. Reprod., November 1, 1999; 14(11): 2731 - 2734.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
Y.M. van Kasteren, R.D.L. Hundscheid, A.P.T. Smits, F.P.M. Cremers, P. van Zonneveld, and D.D.M. Braat
Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease?
Hum. Reprod., October 1, 1999; 14(10): 2455 - 2459.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
A. Murray, J. Webb, F. MacSwiney, E. L. Shipley, N. E. Morton, and G. S. Conway
Serum concentrations of follicle stimulating hormone may predict premature ovarian failure in FRAXA premutation women
Hum. Reprod., May 1, 1999; 14(5): 1217 - 1218.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
A. Marozzi, L. Dalpra, E. Ginelli, M. G. Tibiletti, P. G. Crosignani, and G. S. Conway
FRAXA premutations are not a cause of familial premature ovarian failure
Hum. Reprod., February 1, 1999; 14(2): 573 - 575.
[Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.