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The Role of Genetic Factors in the Development of Epilepsy in the Kazakh Population

Epilepsy Clinical Trial

Official title:
Preventive and Personalized Medicine (2021-2023)

Clinical Trial Summary

This is a GWAS study that aims to identify possible candidate genes associate to epilepsy by exploring single nucleotide polymorphism (SNP) in a group of epilepsy, in the Kazakh population. The investigators hypothesize that the careful phenotyping of the subject sand matching with increase the power to find SNP significantly associate with epilepsy

Clinical Trial Description

A genome-wide association study (GWAS) is an approach used in genetics research to associate specific genetic variations with particular diseases. The method involves scanning the genomes from many different people and looking for genetic markers that can be used to predict the presence of a disease. Once such genetic markers are identified, they can be used to understand how genes contribute to the disease and develop better prevention and treatment strategies ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05088499
Study type Observational
Source Asfendiyarov Kazakh National Medical University
Contact
Status Completed
Phase
Start date February 1, 2022
Completion date January 20, 2023
View Details
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