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| Title: | Hereditary spherocytosis[case study] |
| Authors: | Huq, Sayeeda
Pietroni, Mark A.C.
Rahman, Hafizur
Alam, Mohammad Tariqul |
| Keywords: | Diagnosis, Differential
Female
Folic Acid
Hemoglobins
Hepatomegaly
Leukocyte Count
Oryza sativa
Sodium Chloride
Spherocytosis, Hereditary
Splenomegaly
Vitamin B Complex
Child
Abdomen/
Bangladesh |
| Issue Date: | Feb-2010 |
| Citation: | J Health Popul Nutr 2010 Feb;28(1):107-9 |
| Abstract: | A 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 Bangladesh |
| URI: | http://hdl.handle.net/123456789/3038 |
| Appears in Collections: | Clinical sciences research papers
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Files in This Item:
| File |
Description |
Size | Format |
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| 2010-JHPN-107-HuqS.pdf | | 162Kb | Adobe PDF | View/Open |
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