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.

Unconjugated hyperbilirubinemia

An increased amount of unconjugated (indirect) bilurubin in the blood.


Total: 2

                       


(per page)
PMID (PMCID)
29200157
 FEMALE Infant
An Infant With Unusually High Unconjugated Hyperbilirubinemia Due to Coexistence of Hereditary Spherocytosis and Gilbert Syndrome.
Butorac Ahel I, Baraba Dekanic K, Palcevski G, Roganovic J.
J Pediatr Hematol Oncol. 2018;40(2):e127-e128.
An Infant With Unusually High Unconjugated Hyperbilirubinemia Due to Coexistence of Hereditary Spherocytosis and Gilbert Syndrome.
22134611
 MALE Child
Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis.
Kumar D, Parakh A, Sharma S.
J Pediatr Hematol Oncol. 2012;34(1):54-6.
Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis.