نمایش مختصر رکورد

dc.contributor.authorFekri, ARen_US
dc.contributor.authorShamsaddini, Sen_US
dc.contributor.authorMaghsoodloo Nejad, Aen_US
dc.date.accessioned1399-07-08T19:49:59Zfa_IR
dc.date.accessioned2020-09-29T19:49:59Z
dc.date.available1399-07-08T19:49:59Zfa_IR
dc.date.available2020-09-29T19:49:59Z
dc.date.issued2000-07-01en_US
dc.date.issued1379-04-11fa_IR
dc.identifier.citationFekri, AR, Shamsaddini, S, Maghsoodloo Nejad, A. (2000). Skin and mucous membrane lesions in major B-Thalassemia. Iranian Journal of Dermatology, 3(4), 7-17.en_US
dc.identifier.issn2717-0721
dc.identifier.urihttp://iranjd.ir/article_98392.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/75334
dc.description.abstractBackground: Beta-thalassemia major (BTM) is a genetic disorder, which is common in Kerman province of Iran. New methods of care has increased their survival. Objective: The objective of this descriptive study was to assess the frequency of skin and mucosal complications of BTM patients. Patients and Methods: All BTM patients referred to Kerman-Darman Hospital in 1377 (150 cases) were evaluated. Dermatologic signs and symptoms were diagnosed by physical examination and serum ferritin levels were measured. Results: Skin hyperpigmentation (65.3%), mucosal hyperpigmentation (41.3%), coarse nail (34%) and coarse hair (20.7%) were the most common signs. They were related to the age and serum ferritin levels but sex of patients and dose of desferral had no significant relation with skin complications. Conclusion: Skin and mucosal lesions are common in BTM. An exact exam and control of serum ferritin level with desferral is recommended to prevent skin complications.en_US
dc.format.extent1857
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherIranian Society of Dermatologyen_US
dc.relation.ispartofIranian Journal of Dermatologyen_US
dc.subjectThalassemiaen_US
dc.subjectSkin lesionsen_US
dc.subjectKermanen_US
dc.subjectIranen_US
dc.titleSkin and mucous membrane lesions in major B-Thalassemiaen_US
dc.typeTexten_US
dc.citation.volume3
dc.citation.issue4
dc.citation.spage7
dc.citation.epage17


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