1996
DOI: 10.5144/0256-4947.1996.560
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ß-Thalassemia Major: Experience at King Fahad Hofuf Hospital, Al-Hassa, Saudi Arabia

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Cited by 6 publications
(5 citation statements)
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“…These include neurological disorders, imbalances in electrolytes, viral infections, developmental delays, and elevated levels of cytokines [2]. Similar to Joshi-Batajoo et al [35], Laditan et al [45], and Tavassoli et al [36], none of the patients with BM had meningeal irritation signs in our study, implying that the lack of these signs does not exclude BM in children. Clinicians should not rely solely on physical signs in this regard.…”
Section: Discussionsupporting
confidence: 73%
“…These include neurological disorders, imbalances in electrolytes, viral infections, developmental delays, and elevated levels of cytokines [2]. Similar to Joshi-Batajoo et al [35], Laditan et al [45], and Tavassoli et al [36], none of the patients with BM had meningeal irritation signs in our study, implying that the lack of these signs does not exclude BM in children. Clinicians should not rely solely on physical signs in this regard.…”
Section: Discussionsupporting
confidence: 73%
“…The reduction in blood transfusion requirements from every 2 weeks before splenectomy to every 4 weeks afterwards and the reduction of annual transfusion requirements by 60% are consistent with other reports. 13 All the patients developed thrombocytosis ranging from 500,000 to 1,000,000/mm 3 but required no intervention, as observed by Sumer et al 9 There were no deaths among our children.…”
Section: Discussionsupporting
confidence: 57%
“…10,11 The prevalence of splenectomy among our children with thalassaemia is 32%, similar to other reports from Saudi Arabia. 12,13 Some patients included in the study attended before the establishment of the thalassaemia centre and were not on the hypertransfusion regimen, and some showed poor compliance, resulting in signi cant splenomegaly and hypersplenism. There were no signi cant sex differences.…”
Section: Discussionmentioning
confidence: 99%
“…Jaundice and failure to thrive result in growth retardation and recunent attacks of inf'ections, which are due to impaired neurophil chemotaxis and altered T and B lymphocytes percentages. Thalassaemia patients suffer lrom repeated attack of infection by Yersinia microorganism enhanced by iron overload and immunological defect (2,5,6). Also the measurements of the activity of enzymes in blood are considered a good value in the diagnosis and management and in the monitoring of the case progress of thalassaemia major (7).…”
Section: Introductionmentioning
confidence: 99%