Publication:
Compound Heterozygous Sickle and Thalassemia Trait: A Case Report

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorShrestha, Bikash
dc.contributor.authorKarmacharya, Kavita
dc.contributor.authorSingh, Jasjit
dc.contributor.authorKotwal, Jyoti
dc.contributor.authorDevgan, Amit
dc.date.accessioned2026-06-02T08:07:49Z
dc.date.available2026-06-02T08:07:49Z
dc.date.issued2011
dc.descriptionBikash Shrestha Resident, Department of Pediatrics, Armed Forces Medical College, Pune Kavita Karmacharya Department of Pathology, Armed Forces Medical, College, Pune Jasjit Singh Department of Medicine, Clinical Hematology and Oncology, Command Hospital, Southern Command, Pune Jyoti Kotwal Associate Professor and Senior Advisor, Department of Pathology, Armed Forces Medical, College, Pune Amit Devgan Associate Professor, Department of Pediatrics, Armed Forces Medical College, Pune, India
dc.description.abstractAbstract: Sickle cell disease is a type of hemoglobinopathy, which is fairly common in certain parts of the world. We would like to report an interesting case of a child who was labeled as sickle cell anemia but subsequently turned out to be a case of compound heterozygous sickle cell and thalassemia trait.
dc.identifierhttps://doi.org/10.3126/jnps.v31i2.4414
dc.identifier.urihttps://hdl.handle.net/20.500.14572/6331
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectSickle cell disease
dc.subjecthemoglobinopathy
dc.subjectthalassemia
dc.subjecthydroxyurea
dc.subjectglobin
dc.subjectelectrophoresis
dc.subjectHPLC
dc.titleCompound Heterozygous Sickle and Thalassemia Trait: A Case Report
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage133
oaire.citation.startPage130
relation.isJournalIssueOfPublicatione43eed01-15df-428a-b74c-608eef074322
relation.isJournalIssueOfPublication.latestForDiscoverye43eed01-15df-428a-b74c-608eef074322
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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