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.

Diabetes mellitus

A group of abnormalities characterized by hyperglycemia and glucose intolerance.

Total: 1

(per page)

PMID (PMCID)
17204741	FEMALE	Adult
	Delay in diagnosis of diabetes mellitus due to inaccurate use of hemoglobin A1C levels.
	Arnold JG, McGowan HJ. J Am Board Fam Med. 2007;20(1):93-6.
	Presented is the case of a patient with diabetes mellitus and hereditary spherocytosis, a condition that interfered with her HbA(1C) value and resulted in a delay in her care.