Hereditary spherocytosis[case study]

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dc.contributor.authorHuq, Sayeeda-
dc.contributor.authorPietroni, Mark A.C.-
dc.contributor.authorRahman, Hafizur-
dc.contributor.authorAlam, Mohammad Tariqul-
dc.date.accessioned2011-08-17T03:21:44Z-
dc.date.available2011-08-17T03:21:44Z-
dc.date.issued2010-02-
dc.identifier.citationJ Health Popul Nutr 2010 Feb;28(1):107-9en
dc.identifier.urihttp://hdl.handle.net/123456789/3038-
dc.description.abstractA 12-year-old girl was brought to the Dhaka Hospital of ICDDR,B with diarrhoea. Incidentally, the parents provided a history of repeated episodes of pallor and jaundice since she was two and half years old. Three of her family members had similar problems. History, clinical examination, and laboratory findings of the girl and her family members suggested a case of hereditary spherocytosis. To our knowledge, this is the first report of such a case in Bangladeshen
dc.format.extent166582 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoenen
dc.subjectDiagnosis, Differentialen
dc.subjectFemaleen
dc.subjectFolic Aciden
dc.subjectHemoglobinsen
dc.subjectHepatomegalyen
dc.subjectLeukocyte Counten
dc.subjectOryza sativaen
dc.subjectSodium Chlorideen
dc.subjectSpherocytosis, Hereditaryen
dc.subjectSplenomegalyen
dc.subjectVitamin B Complexen
dc.subjectChilden
dc.subjectAbdomen/en
dc.subjectBangladeshen
dc.titleHereditary spherocytosis[case study]en
dc.typeArticleen
Appears in Collections:Clinical sciences research papers

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