Night Eating Syndrome: Report of a family case

dc.authoridAllison, Kelly C./0000-0002-9807-0220
dc.authoridSevincer, Guzin Mukaddes/0000-0001-6081-6325
dc.contributor.authorSevincer, Guzin M.
dc.contributor.authorAllison, Kelly C.
dc.date.accessioned2024-09-11T19:50:52Z
dc.date.available2024-09-11T19:50:52Z
dc.date.issued2016
dc.departmentİstanbul Gelişim Üniversitesien_US
dc.description.abstractNight eating syndrome (NES) represents a circadian delay in the pattern of eating. As there are genetic links for other eating- and circadian-based disorders, it is likely that there is a genetic basis for NES as well. We present a family case study of three identified patients and their extensive family history of NES and co-morbid mood disorders. This case report suggested that NES may have a heritable feature, particularly nocturnal ingestions. Of the seven identified cases, four had co-morbid mood disorders, and all descended from a couple with bipolar disorder and delusional disorder. More work is needed to understand the extent of genetic influence on NES, and the relationship between NES and other psychiatric disorders. (C) 2016 Elsevier Ltd. All rights reserved.en_US
dc.identifier.doi10.1016/j.eatbeh.2016.03.022
dc.identifier.endpage86en_US
dc.identifier.issn1471-0153
dc.identifier.issn1873-7358
dc.identifier.pmid27093391en_US
dc.identifier.scopus2-s2.0-84963690365en_US
dc.identifier.startpage83en_US
dc.identifier.urihttps://doi.org/10.1016/j.eatbeh.2016.03.022
dc.identifier.urihttps://hdl.handle.net/11363/7693
dc.identifier.volume22en_US
dc.identifier.wosWOS:000381254700015en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofEating Behaviorsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.snmz20240903_Gen_US
dc.subjectNight Eating Syndromeen_US
dc.subjectFamilialen_US
dc.subjectGeneticen_US
dc.titleNight Eating Syndrome: Report of a family caseen_US
dc.typeArticleen_US

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