Evaluation of patients diagnosed with congenital hypothyroidism by newborn screening between 2011-2019 in Diyarbakir, Turkey

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dc.authorid0000-0002-3616-9399en_US
dc.authorscopusid57189501874en_US
dc.authorwosidGQB-0856-2022en_US
dc.contributor.authorToktaş, İzzettin
dc.contributor.authorErdem, Özgür
dc.contributor.authorSarıbaş, Seyfettin
dc.contributor.authorÖzbek, Mehmet Nuri
dc.date.accessioned2023-12-25T12:32:16Z
dc.date.available2023-12-25T12:32:16Z
dc.date.issued2023en_US
dc.departmentMAÜ, Fakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Halk Sağlığı Ana Bilim Dalıen_US
dc.description.abstractThis study aimed to determine the incidence of congenital hypothyroidism in Turkey’s Diyarbakir Province and assess the development and growth conditions of people with congenital hypothyroidism. Patients born between 2011-2019 and diagnosed with congenital hypothyroidism within the scope of the newborn screening program were included. The medical records of these patients were retrospectively reviewed. The length and weight for age, weight for length, and body mass index standard deviation scores were calculated. We investigated the treatment status of the patients, whether their relatives had a similar disorder, and the presence of consanguinity between parents. Blood samples were collected from 380,592 newborns. As a result of further tests, 498 newborns were diagnosed with congenital hypothyroidism (incidence: 1/764). Demographic and anthropometric data of 241 patients were analyzed. The patients comprised 46.9% (n = 113) females and 53.1% (n = 128) males. It was determined that 44.4% of the individuals had transient congenital hypothyroidism and 53.6% had permanent congenital hypothyroidism. The parents of 29.8% of the individuals diagnosed with transient congenital hypothyroidism and 44.2% of the individuals diagnosed with permanent congenital hypothyroidism were consanguineous (P = .02). According to the latest anthropometric assessment, 6.8% of individuals diagnosed with congenital hypothyroidism had a weight z-score below −2 SD and 16.9% had a length z-score below −2 SD. The incidence of congenital hypothyroidism was higher in our region. The ratio of consanguinity between parents was higher in patients diagnosed with permanent congenital hypothyroidism than in those diagnosed with transient congenital hypothyroidism. According to the most recent follow-up, weight and age were found to be similar in patients with transient and permanent congenital hypothyroidism.en_US
dc.identifier.doi10.1097/MD.0000000000036778en_US
dc.identifier.endpage5en_US
dc.identifier.issue51en_US
dc.identifier.pmid38134076en_US
dc.identifier.scopus2-s2.0-85180979051en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage1en_US
dc.identifier.urihttp://doi.org/10.1097/MD.0000000000036778
dc.identifier.urihttps://hdl.handle.net/20.500.12514/5192
dc.identifier.volume102en_US
dc.identifier.wosWOS:001130483000054en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.institutionauthorToktaş, İzzettin
dc.institutionauthorÖzbek, Mehmet Nuri
dc.language.isoenen_US
dc.publisherLWWen_US
dc.relation.ispartofMedicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBody heighten_US
dc.subjectBody weight
dc.subjectCongenital hypothyroidism
dc.subjectIncidence
dc.subjectInfant
dc.titleEvaluation of patients diagnosed with congenital hypothyroidism by newborn screening between 2011-2019 in Diyarbakir, Turkeyen_US
dc.typeArticleen_US

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