Cystic fibrosis diagnosed in a nineteen-year-old case

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dc.contributor.authorYılmaz, Meltem
dc.contributor.authorMutlu, Levent Cem
dc.date.accessioned2024-10-29T17:50:02Z
dc.date.available2024-10-29T17:50:02Z
dc.date.issued2023
dc.departmentTekirdağ Namık Kemal Üniversitesien_US
dc.description.abstractCystic fibrosis is the most common autosomal recessive hereditary disease in white populations. It is characterized by the formation of abnormal secretions in the exocrine glands located in the sweat and salivary glands, tracheobronchial tree, large intestine, and pancreas. The severity of the clinic depends on the type of \"cystic fibrosis transmembrane regulatory protein\" gene mutation. Although most cases are diagnosed in infancy or childhood, some patients are also diagnosed during adolescence and adulthood. We report a case of a 19-year-old patient who was followed up with a diagnosis of asthma and bronchiectasis since childhood and diagnosed with cystic fibrosis.en_US
dc.identifier.doi10.18621/eurj.1207253
dc.identifier.endpage1540en_US
dc.identifier.issn2149-3189
dc.identifier.issue6en_US
dc.identifier.startpage1537en_US
dc.identifier.trdizinid1207268en_US
dc.identifier.urihttps://doi.org/10.18621/eurj.1207253
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/1207268
dc.identifier.urihttps://hdl.handle.net/20.500.11776/12730
dc.identifier.volume9en_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.relation.ispartofThe European Research Journalen_US
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAdolescenceen_US
dc.subjectbronchiectasisen_US
dc.subjectcystic fibrosisen_US
dc.titleCystic fibrosis diagnosed in a nineteen-year-old caseen_US
dc.typeArticleen_US

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