Female sex preponderance for idiopathic familial premature ovarian failure suggests an X chromosome defect

被引:56
作者
Davis, CJ [1 ]
Davison, RM
Payne, NN
Rodeck, CH
Conway, GS
机构
[1] UCL Hosp, Dept Obstet & Gynaecol, London W1N 8AA, England
[2] UCL Hosp, Dept Endocrinol, London W1N 8AA, England
[3] Middlesex Hosp, Cobbold Labs, London W1N 8AA, England
关键词
BPES; FRAXA premutation; premature ovarian failure; X chromosome;
D O I
10.1093/humrep/15.11.2418
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Premature ovarian failure (POF) is defined as ovarian failure occurring before the age of 40 years, A genetic aetiology is suggested by the occurrence of families with two or more affected females. We have characterised the pattern of inheritance of 41 cases of familial POF and compared them to published pedigrees, In eleven families a clear genetic association of POF could be identified. In the remaining 30 families the mechanism of inheritance was obscure. We found a female sex preponderance in the siblings of 30 families with idiopathic POF and in previously published series of idiopathic familial POF, In contrast, other known causes of POF, such as blepharophimosis ptosis epicanthus and inversus and autosomal recessive gonadal dysgenesis, had no altered sex ratio. One of our series of 30 pedigrees demonstrated transmission of POF susceptibility through fathers, which vee believe is the first to be described in the literature. We present a group of five consanguineous families where we assume the mode of inheritance is autosomal recessive and where there was no female sex preponderance. Female ses preponderance for idiopathic familial POF suggests an X chromosome defect is inherited as a major cause of ovarian failure.
引用
收藏
页码:2418 / 2422
页数:5
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