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.

Hypophosphatemia

An abnormally decreased phosphate concentration in the blood.

Total: 1

(per page)

PMID (PMCID)
9637890	MALE	Adult
	[Hereditary spherocytosis associated with severe hypophosphatemia in patients recovering from aplastic crisis].
	Sahara N, Tamashima S, Ihara M. Rinsho Ketsueki. 1998;39(5):386-91.
	This is a report about two cases of hereditary spherocytosis complicated by severe hypophosphatemia, while recovering from aplastic crisis.