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Silent Stroke in a Case of Β-Thalassemia Major Associated With Chronic Renal Failure and Diabetes Mellitus

dc.authorscopusid 7101974609
dc.authorscopusid 7003543848
dc.authorscopusid 6602406361
dc.authorscopusid 7005791514
dc.authorscopusid 7006604555
dc.authorscopusid 6603814316
dc.authorscopusid 6603814316
dc.authorwosid Odabaş, Dursun/Mbh-2762-2025
dc.authorwosid Arslan, Şükrü/Abc-4250-2021
dc.authorwosid Akbayram, Sinan/Aag-5737-2020
dc.contributor.author Çaksen, H
dc.contributor.author Odabas, D
dc.contributor.author Akbayram, S
dc.contributor.author Öner, AF
dc.contributor.author Arslan, S
dc.contributor.author Cesur, Y
dc.contributor.author Üner, A
dc.date.accessioned 2025-05-10T17:38:58Z
dc.date.available 2025-05-10T17:38:58Z
dc.date.issued 2003
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp Yuzuncu Yyl Univ, Fac Med, Dept Pediat, Van, Turkey en_US
dc.description.abstract Severe anemia, growth retardation, diabetes mellitus, cardiac disorders, and, infrequently, stroke are well-known complications of thalassemia major. We report a girl, age 7 years, 2 months, with beta-thalassemia major associated with chronic renal failure, diabetes mellitus, and cardiomyopathy in whom a silent stroke was noted during follow-up. She was diagnosed with thalassemia major at age 6 months, chronic renal failure at age 3 years, 3 months, and diabetes mellitus and cardiomyopathy at age 7 years. Although cranial computed tomography was found to be normal at the age of 3 years, 3 months, magnetic resonance imaging showed cerebral infarct in the right frontal region at 7 years, 2 months. A thrombophilic panel revealed increased factor VIII and decreased protein C concentrations. She died from disseminated intravascular coagulation at age 7 years, 9 months. We did not record any clinical findings of stroke during her follow-up. We think that diabetes mellitus, dilated cardiomyopathy, and increased factor VIII and decreased protein C concentrations led to the occurrence of cerebral infarct. In conclusion, we emphasize that children with thalassemia major should be monitored closely for stroke. We also suggest that stroke can show a silent progression in severely affected children, as in our case. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.1177/08830738030180110201
dc.identifier.endpage 800 en_US
dc.identifier.issn 0883-0738
dc.identifier.issue 11 en_US
dc.identifier.pmid 14696909
dc.identifier.scopus 2-s2.0-0347513292
dc.identifier.scopusquality Q2
dc.identifier.startpage 798 en_US
dc.identifier.uri https://doi.org/10.1177/08830738030180110201
dc.identifier.uri https://hdl.handle.net/20.500.14720/14751
dc.identifier.volume 18 en_US
dc.identifier.wos WOS:000187437400013
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.publisher B C decker inc en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.title Silent Stroke in a Case of Β-Thalassemia Major Associated With Chronic Renal Failure and Diabetes Mellitus en_US
dc.type Article en_US

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