Please use this identifier to cite or link to this item: http://repository.kln.ac.lk/handle/123456789/18601
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dc.contributor.authorPremathilaka, L.H.R.A.-
dc.contributor.authorLakmini, M.S.-
dc.contributor.authorThamal Dharshana, L.G.-
dc.contributor.authorNawaratne, S.B.-
dc.contributor.authorMettananda, S.-
dc.contributor.authorde Silva, S.T.-
dc.contributor.authorPremawardhena, A.P.-
dc.date.accessioned2018-02-08T04:36:22Z-
dc.date.available2018-02-08T04:36:22Z-
dc.date.issued2017-
dc.identifier.citationSri Lanka Journal of Medicine.2017;26(2):55–57en_US
dc.identifier.issn2579-1990-
dc.identifier.urihttp://repository.kln.ac.lk/handle/123456789/18601-
dc.description.abstractStroke in Sickle cell disease is a devastating complication. As Sickle cell disease is uncommon in Sri Lanka many clinicians may be unfamiliar with management of the disease and its complications. A 10-year-old boy presented with a transient ischaemic attack. He has had a silent large parietal infarct previously. He had been managed with transfusions and had undergone a splenectomy. However, he had not received hydroxyurea or undergone trans-cranial Doppler assessment.en_US
dc.language.isoen_USen_US
dc.publisherKandy Society of Medicineen_US
dc.subjectSickle beta thalassemiaen_US
dc.titleStroke in sickle cell beta thalassemia - a case report highlighting pitfalls in management in a low prevalence countryen_US
dc.typeArticleen_US
Appears in Collections:Journal/Magazine Articles

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