Hereditary spherocytosis

Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum (from symptom-free carriers to severe hemolysis) characterized by anemia, variable jaundice, splenomegaly and cholelithiasis.

Lethargy

A state of disinterestedness, listlessness, and indifference, resulting in difficulty performing simple tasks or concentrating.


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PMID (PMCID)
26139647
 MALE
An adolescent with hereditary spherocytosis who presented with splenic infarction.
Jones L, Refai Z, Linney M.
BMJ Case Rep. 2015;2015:.
A 16-year-old male patient with known hereditary spherocytosis presented with a 4-day history of chest pain and lethargy.