Article:
A Child Lost to Follow Up Carrying Beta Thalassemia Major: A Case Report

creativeworkseries.issnJNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X
dc.contributor.authorBanjade, Prakash
dc.contributor.authorBhandari, Jeetendra
dc.date.accessioned2026-08-11T05:52:04Z
dc.date.available2026-08-11T05:52:04Z
dc.date.issued2020
dc.descriptionPrakash Banjade Department of Internal Medicine, Gan Regional Hospital, Maavah Health Center, Republic of Maldives Jeetendra Bhandari Department of Emergency Medicine, Chitwan Medical College, Chitwan, Nepal
dc.description.abstractAbstract Thalassemia is inherited autosomal recessive disorders characterized by reduced rate of hemoglobin synthesis due to a defect in alpha or beta globin chain synthesis. Maldives has a beta thalassemia prevalence rate of 16-18%. Classical symptoms of beta thalassemia are common on those patients who present late for blood transfusion which is common among the south Asian countries due to resource poor situation. This case is a rare case report of commonly occurring phenomenon which has been reported less among south Asian region. Reporting this case will help health worker to manage cases accordingly. A five and half year prior diagnosed case of beta thalassemia at age of 2 years and lost to follow up presented with cough, Dyspnoea, Irritability, fatigue with classic symptom of beta thalassemia. She was managed with blood transfusion and kept on continuous follow up for transfusion and iron overload management. Keywords: Beta Thalassemia, case report, follow up, Maldives
dc.identifierhttps://doi.org/10.31729/jnma.5129
dc.identifier.urihttps://hdl.handle.net/20.500.14572/7204
dc.language.isoen_US
dc.publisherNepal Medical Association
dc.subjectBeta Thalassemia
dc.subjectcase report
dc.subjectfollow up
dc.subjectMaldives
dc.titleA Child Lost to Follow Up Carrying Beta Thalassemia Major: A Case Report
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage438
oaire.citation.startPage436
relation.isJournalIssueOfPublication68e7987e-f8d8-4254-97f6-36ef07649cc0
relation.isJournalIssueOfPublication.latestForDiscovery68e7987e-f8d8-4254-97f6-36ef07649cc0
relation.isJournalOfPublicatione6e146a0-0ece-4aba-aa0a-6ccfbd10a12a

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