Total: 1 |
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PMID (PMCID) | ||
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27423290 |
MALE | Child |
Hereditary Spherocytosis with Splenomegaly and Cholelithiasis in a Young Male of Western Region of Nepal - A Case Report. | ||
Ghimire P, Gurung NV, Shrestha S, Poudel SR, Chapagain A. Kathmandu Univ Med J (KUMJ). 2015;13(52):366-8. |
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Hereditary spherocytosis is an autosomal dominant congenital hemolytic anemia due to defect in RBC membrane protein that commonly presents with intermittent jaundice, anemia, abdominal pain, splenomegaly and sometimes cholelithiasis. |