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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.

Acute encephalopathy

Total: 1

(per page)

PMID (PMCID)
18520445	FEMALE	Child
	Acute encephalopathy with human parvovirus B19 infection in hereditary spherocytosis.
	Oshima K, Kikuchi A, Mochizuki S, Arai T, Oishi T, Hanada R. Pediatr Infect Dis J. 2008;27(7):651-2.
	Acute encephalopathy with human parvovirus B19 infection in hereditary spherocytosis.