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dc.contributor.authorIşık, Pamir
dc.contributor.authorYaralı, Neşe
dc.contributor.authorTavil, Betül
dc.contributor.authorDemirel, Fatma
dc.contributor.authorKaraçam, Gülşah Bayram
dc.contributor.authorSaç, Rukiye Ünsal
dc.contributor.authorFettah, Ali
dc.contributor.authorÖzkasap, Serdar
dc.contributor.authorKara, Abdurrahman
dc.contributor.authorTunç, Bahattin
dc.date.accessioned2020-12-19T20:15:51Z
dc.date.available2020-12-19T20:15:51Z
dc.date.issued2014
dc.identifier.citationIsik, P., Yarali, N., Tavil, B., Demirel, F., Karacam, G. B., Sac, R. U., Fettah, A., Ozkasap, S., Kara, A., & Tunc, B. (2014). Endocrinopathies in Turkish children with Beta thalassemia major: results from a single center study. Pediatric hematology and oncology, 31(7), 607–615. https://doi.org/10.3109/08880018.2014.898724en_US
dc.identifier.issn0888-0018
dc.identifier.urihttps://doi.org/10.3109/08880018.2014.898724
dc.identifier.urihttps://hdl.handle.net/11436/4051
dc.descriptionPubMed: 24854890en_US
dc.description.abstractThe endocrinological complications in ?-thalassemia major patients do affect the life quality to a large extend. In this study, the endocrinological complications of 47 ?-thalassemia patients, who have been followed-up at our hospital's pediatric hematology department, were evaluated. Out of ?-thalassemia major cases included to this study, the 55.3% was male and 44.7% was female. The patients' mean levels of ferritin, whose mean age was 10.0 ± 4.5 years (2-20 years), were 2497 ± 1469 ng/mL (472-8558 ng/mL). At least one endocrinological pathology in 27 out of 47 (57.4%) and more than one endocrinological pathology in 14 out of 47 (29.7%) thalassemia patients were observed. The most frequently observed complication in followed-up cases was vitamin D insufficiency and deficiency (78.2%). The other complications in decreasing order were pubertal failure (41.6%), growth retardation (25.5%), decreased bone-mineral density (22.2%), secondary hyperparathyroidism (11.5%), overt hypothyroidism (4.25%), subclinical hypothyroidism (2.12%), and impaired glucose tolerance (2.12%). There was no statistically significant difference between serum mean ferritin level and endocrin complications (P > .05). Four patients (8.5%) had decreased signal intensity in pituitary magnetic resonance imaging (MRI) but this finding was not associated with ferritin levels (P = .87). MRI parameters were similar between patients with and without gonadal dysfunction. Mean height of the pituitary gland was 4.98 ± 1.1 mm (3-9 mm) and this was similar to those normal values in the literature. Ferritin levels were not correlated with pituitary height (P > .05). Beta thalassemia major, having the potential of leading to multisystemic complications, is a chronic disease that should be treated and followed-up by a multidisciplinary approach. Due to frequently encountered endocrinological complications, beta thalassemic patients should be followed-up regularly by hematology and endocrinology departments in coordination. © 2014 Informa Healthcare USA, Inc.en_US
dc.language.isoengen_US
dc.publisherInforma Healthcareen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEndocrinologyen_US
dc.subjectPediatricsen_US
dc.subjectRadiologyen_US
dc.subjectThalassemiaen_US
dc.titleEndocrinopathies in Turkish children with beta thalassemia major: Results from a single center studyen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.contributor.institutionauthorÖzkasap, Serdar
dc.identifier.doi10.3109/08880018.2014.898724
dc.identifier.volume31en_US
dc.identifier.issue7en_US
dc.identifier.startpage607en_US
dc.identifier.endpage615en_US
dc.relation.journalPediatric Hematology and Oncologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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