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Genetic Etiology in Premature Ovarian Insufficiency — POI  

Genetic Predisposition to Disease Clinical Trial

Official title:
Genetic Etiology in Premature Ovarian Insufficiency

Clinical Trial Summary

Premature Ovarian Insufficiency (POI), first described by Albright in 1942, is defined as an increase in Follicle Stimulating Hormone (FSH), an insufficiency of the ovarian function leading to an early menopause (<40 years of age).Today, only 35% of POI's etiology can be explained. Causes enlightening POI may be enumerated as follows, according to their frequency: genetic mutations, autoimmune defects and abnormalities detected on the X chromosome.The purpose of the study is to determine the frequency of the genetic abnormalities and polymorphisms described above in the POI Turkish population

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01973075
Study type Observational [Patient Registry]
Source Sisli Etfal Training & Research Hospital
Contact
Status Completed
Phase N/A
Start date November 2013
Completion date April 2017
View Details
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