Document Detail


Female sex preponderance for idiopathic familial premature ovarian failure suggests an X chromosome defect: opinion.
MedLine Citation:
PMID:  11056145     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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 we 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 sex preponderance for idiopathic familial POF suggests an X chromosome defect is inherited as a major cause of ovarian failure.
Authors:
C J Davis; R M Davison; N N Payne; C H Rodeck; G S Conway
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Publication Detail:
Type:  Journal Article; Review    
Journal Detail:
Title:  Human reproduction (Oxford, England)     Volume:  15     ISSN:  0268-1161     ISO Abbreviation:  Hum. Reprod.     Publication Date:  2000 Nov 
Date Detail:
Created Date:  2000-11-27     Completed Date:  2000-12-22     Revised Date:  2005-11-16    
Medline Journal Info:
Nlm Unique ID:  8701199     Medline TA:  Hum Reprod     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  2418-22     Citation Subset:  IM    
Affiliation:
Department of Obstetrics and Gynaecology, Department of Endocrinology, University College Hospital London, The Cobbold Laboratories, Middlesex Hospital, London W1N 8AA, UK. c8davis@aol.com
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MeSH Terms
Descriptor/Qualifier:
Chromosome Aberrations / genetics
Chromosome Disorders
Consanguinity
Female
Humans
Ovarian Failure, Premature / genetics*
Pedigree
Sex Ratio*
X Chromosome / genetics*

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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