Document Detail


Polycystic ovary syndrome: an ancient disorder?
MedLine Citation:
PMID:  20979996     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Polycystic ovary syndrome (PCOS) appears to be an ancient disorder, which has persisted in human evolution despite reduced fecundity because of the benefits to affected women such as greater sturdiness and improved energy utilization, a rearing advantage for their children and kin, and a reduction in the risk of perinatal mortality. This raises the possibility that gene variants that are eventually found to be associated with PCOS will be similar across ethnic groups and races.
Authors:
Ricardo Azziz; Daniel A Dumesic; Mark O Goodarzi
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Publication Detail:
Type:  Historical Article; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review     Date:  2010-10-27
Journal Detail:
Title:  Fertility and sterility     Volume:  95     ISSN:  1556-5653     ISO Abbreviation:  Fertil. Steril.     Publication Date:  2011 Apr 
Date Detail:
Created Date:  2011-03-22     Completed Date:  2011-05-11     Revised Date:  2012-04-04    
Medline Journal Info:
Nlm Unique ID:  0372772     Medline TA:  Fertil Steril     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1544-8     Citation Subset:  IM    
Copyright Information:
Copyright © 2011 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.
Affiliation:
Department of Obstetrics and Gynecology, Cedars-Sinai Medical Center, Los Angeles, California, USA. razziz@mcg.edu
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MeSH Terms
Descriptor/Qualifier:
Continental Population Groups / genetics
Female
Genetic Predisposition to Disease / ethnology
History of Medicine*
History, Ancient
History, Medieval
Humans
Linkage Disequilibrium
Obesity / complications,  epidemiology,  ethnology
Polycystic Ovary Syndrome* / epidemiology,  ethnology,  etiology,  genetics
Prevalence
Risk Factors
Grant Support
ID/Acronym/Agency:
R01 DK073632-06/DK/NIDDK NIH HHS; R01 HD029364-14/HD/NICHD NIH HHS; R01 HD029364-15/HD/NICHD NIH HHS; R01-DK79888/DK/NIDDK NIH HHS; R01-HD29364/HD/NICHD NIH HHS

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


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