Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

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.

Chronic hemolytic anemia

An chronic form of hemolytic anemia.

Total: 1

(per page)

PMID (PMCID)
3020677	MIXED_SAMPLE	Adult
	Inhibition of erythropoiesis by human parvovirus-containing serum from a patient with hereditary spherocytosis in aplastic crisis.
	Takahashi M, Koike T, Moriyama Y, Shibata A, Koike R, Sanada M, Tsukada T. Scand J Haematol. 1986;37(2):118-24.
	The results suggested that aplastic crisis of a patient with hereditary spherocytosis is caused by human parvovirus and that the neutralizing test could offer a tool for predicting the future occurrence of aplastic crisis in the patients with chronic hemolytic anemia.