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Confirmation of early menopause in fragile X carriers.

作者信息

Partington M W, Moore D Y, Turner G M

机构信息

Hunter Genetics, Newcastle, New South Wales, Australia.

出版信息

Am J Med Genet. 1996 Aug 9;64(2):370-2. doi: 10.1002/(SICI)1096-8628(19960809)64:2<370::AID-AJMG27>3.0.CO;2-B.

DOI:10.1002/(SICI)1096-8628(19960809)64:2<370::AID-AJMG27>3.0.CO;2-B
PMID:8844083
Abstract

Fragile X carriers have a median age of menopause 6 to 8 years earlier than women in the general population, with 28% experiencing premature ovarian failure defined as menopause before the age of 40 years. This information was obtained from 203 returned questionnaires from women in the UK Fragile X Society.

摘要

相似文献

1
Confirmation of early menopause in fragile X carriers.
Am J Med Genet. 1996 Aug 9;64(2):370-2. doi: 10.1002/(SICI)1096-8628(19960809)64:2<370::AID-AJMG27>3.0.CO;2-B.
2
Premature ovarian failure (POF) and fragile X premutation females: from POF to to fragile X carrier identification, from fragile X carrier diagnosis to POF association data.卵巢早衰（POF）与脆性X前突变女性：从卵巢早衰到脆性X携带者鉴定，从脆性X携带者诊断到卵巢早衰关联数据。
Am J Med Genet. 1999 May 28;84(3):300-3.
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Anti-Mullerian hormone indicates early ovarian decline in fragile X mental retardation (FMR1) premutation carriers: a preliminary study.抗苗勒管激素表明脆性X智力低下（FMR1）前突变携带者存在早期卵巢功能衰退：一项初步研究。
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Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation.关于特发性卵巢早衰与脆性X前突变之间关联中的回忆偏倚。
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Premature ovarian failure and fragile X female premutation carriers: no evidence for a skewed X-chromosome inactivation pattern.卵巢早衰与脆性X女性前突变携带者：不存在X染色体失活模式偏斜的证据。
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Premature ovarian failure in the fragile X syndrome.脆性X综合征中的卵巢早衰。
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[Abnormal function of ovaries in women carriers of premutation in the FMR1 gene].[FMR1基因前突变女性携带者卵巢功能异常]
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Very early premature ovarian failure in two sisters compound heterozygous for the FMR1 premutation.两姐妹因FMR1前突变的复合杂合子导致极早期卵巢早衰。
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引用本文的文献

1
Fragile X-Associated Diminished Ovarian Reserve and Primary Ovarian Insufficiency from Molecular Mechanisms to Clinical Manifestations.脆性X染色体相关的卵巢储备功能减退和原发性卵巢功能不全：从分子机制到临床表现
Front Mol Neurosci. 2017 Sep 12;10:290. doi: 10.3389/fnmol.2017.00290. eCollection 2017.
2
Genetic Counseling for Fragile X Syndrome: Recommendations of the National Society of Genetic Counselors.脆性X综合征的遗传咨询：美国国家遗传咨询师协会的建议
J Genet Couns. 2000 Aug;9(4):303-25. doi: 10.1023/A:1009454112907.
3
FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure.
脆性X智力低下基因1（FMR1）重复序列大小处于灰色区域和正常范围高端与卵巢早衰相关。
Hum Genet. 2005 Aug;117(4):376-82. doi: 10.1007/s00439-005-1326-8. Epub 2005 Jun 2.
4
Reproductive and menstrual history of females with fragile X expansions.具有脆性X染色体扩增的女性的生殖和月经史。
Eur J Hum Genet. 2000 Apr;8(4):247-52. doi: 10.1038/sj.ejhg.5200451.
5
Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations.印记效应在局限于父系遗传的脆性X前突变所致的卵巢早衰中存在。
Am J Hum Genet. 2000 Feb;66(2):413-8. doi: 10.1086/302774.
6
Serum concentrations of follicle stimulating hormone may predict premature ovarian failure in FRAXA premutation women.促卵泡激素的血清浓度可能预示着脆性X前突变女性的卵巢早衰。
Hum Reprod. 1999 May;14(5):1217-8. doi: 10.1093/humrep/14.5.1217.
7
Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data.脆性X前突变是卵巢早衰的一个重要风险因素：脆性X国际卵巢早衰协作研究——初步数据。
Am J Med Genet. 1999 Apr 2;83(4):322-5.
8
Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population.在一个种族多样化、有特殊教育需求的大群体中FRAXA和FRAXE等位基因的患病率及表型后果
Am J Hum Genet. 1999 Feb;64(2):495-507. doi: 10.1086/302260.
9
The fragile X syndrome.脆性X综合征
J Med Genet. 1998 Jul;35(7):579-89. doi: 10.1136/jmg.35.7.579.
10
Fragile X premutations are not a major cause of early menopause.脆性X前突变并非早发性绝经的主要原因。
Am J Hum Genet. 1997 Dec;61(6):1362-9. doi: 10.1086/301647.