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dc.contributor.authorSaǧ, Elif
dc.contributor.authorÇAKIR, MURAT
dc.contributor.authorAkbulut, Ulaş Emre
dc.date.accessioned2022-02-18T09:54:38Z
dc.date.available2022-02-18T09:54:38Z
dc.date.issued2016
dc.identifier.citationSaǧ E., Akbulut U. E. , ÇAKIR M., "The coexistence of cystic fibrosis and celiac disease in a child: Case report Bir çocukta kistik fibrozis ve çölyak hastaliǧi birlikteliǧi", Turkiye Klinikleri Pediatri, cilt.25, sa.3, ss.179-182, 2016
dc.identifier.othervv_1032021
dc.identifier.otherav_6ab5dfbd-97bc-4613-b8f3-a11155672f99
dc.identifier.urihttp://hdl.handle.net/20.500.12627/178232
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84994520386&origin=inward
dc.identifier.urihttps://doi.org/10.5336/pediatr.2016-51222
dc.description.abstract© Copyright 2016 by Türkiye Klinikleri.Cystic fibrosis (CF) is an autosomal recessive disorder characterized by recurrent pulmonary infections, fat malabsorption and growth retardation. The patients are generally treated pancreatic enzyme replacement therapy (PERT) and enteral nutrition support. Optimal growth could not achieved in some patients despite the adequate treatment. These patients must be evaluated for other malabsorption syndromes such as celiac disease (CD). We presented a case to pay attention the presence of CD in a patient with CF who had growth retardation and gastrointestinal symptoms despite adequate PERT and nutritional support.
dc.language.isoeng
dc.subjectHealth Sciences
dc.subjectSağlık Bilimleri
dc.subjectPediatrics, Perinatology and Child Health
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectTıp
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.titleThe coexistence of cystic fibrosis and celiac disease in a child: Case report Bir çocukta kistik fibrozis ve çölyak hastaliǧi birlikteliǧi
dc.typeMakale
dc.relation.journalTurkiye Klinikleri Pediatri
dc.contributor.departmentKaradeniz Teknik Üniversitesi , ,
dc.identifier.volume25
dc.identifier.issue3
dc.identifier.startpage179
dc.identifier.endpage182
dc.contributor.firstauthorID3061147


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