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.

Neonatal hyperbilirubinemia

A type of hyperbilirubinemia with neonatal onset.


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PMID (PMCID)
30207817
 FEMALE Infant, Newborn
Tokyo-1 Mutation: Hereditary Spherocytosis in a Hispanic Newborn Presenting as Early Onset Severe Hyperbilirubinemia.
Tan AW, Leung P, Patil UP.
Fetal Pediatr Pathol. 2018;37(4):296-300.
The absence of a positive family history does not preclude hereditary spherocytosis as a differential for pathologic neonatal hyperbilirubinemia.