Is obesity genetic disease?

dc.contributor.authorDuran, Tugce
dc.contributor.authorZainalbden, Hasanain Akram
dc.contributor.authorKoçak, Nadir
dc.date.accessioned2021-11-26T09:22:12Z
dc.date.available2021-11-26T09:22:12Z
dc.date.issued2017
dc.departmentİnönü Üniversitesien_US
dc.description.abstractAbstract:Obesity is a complex disease that has unfavorable impacts for all ethnic populations in worldwide. Genetics, environment and lifestyle are among aetiological factors of this disease. Genetic contribution associated with this disease is generally classified into 2 types: monogenic syndromes that display severe obesity, and the polygenic model of common obesity. Single-gene mutations can cause severe obesity resulting from alteration in central and peripheral appetite control mechanisms. Candidate gene and genome-wide association studies have led to the identification of nine loci associated with Mendelian forms of obesity and 58 loci contributing to polygenic obesity. These loci explain a small fraction of the heritability for obesity and many genes remain to be identified. The interaction of several polymorphisms and epigenetic modifications open a new research field for common obesity. As a result, still remains to be a mystery.en_US
dc.identifier.citationDURAN T,ZAİNALBDEN H. A,KOÇAK N (2017). Is obesity genetic disease?. İnönü Üniversitesi Turgut Özal Tıp Merkezi Dergisi, 24(4), 531 - 534. Doi: 10.5455/jtomc.2017.03.032en_US
dc.identifier.urihttps://app.trdizin.gov.tr/makale/TWpnME9EUXhNUT09/is-obesity-genetic-disease-
dc.identifier.urihttps://hdl.handle.net/11616/43419
dc.language.isoenen_US
dc.relation.ispartofİnönü Üniversitesi Turgut Özal Tıp Merkezi Dergisien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleIs obesity genetic disease?en_US
dc.typeArticleen_US

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