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.

Hyperamylasemia

Increased level of amylase in the blood, an enzyme which helps digest glycogen and starch. It is produced mainly in the pancreas and salivary glands.


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PMID (PMCID)
6161763
 FEMALE
Hyperamylasemia, duodenal duplication, and pleural effusions in hereditary spherocytosis.
Hyman PE, Brennan MF, Head G, McCarthy DM.
Dig Dis Sci. 1981;26(1):81-4.
Hyperamylasemia, duodenal duplication, and pleural effusions in hereditary spherocytosis.