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.

Cardiomyopathy

A myocardial disorder in which the heart muscle is structurally and functionally abnormal, in the absence of coronary artery disease, hypertension, valvular disease and congenital heart disease sufficient to cause the observed myocardial abnormality.


Total: 3

                       


(per page)
PMID (PMCID)
29140423
 FEMALE
Ventricular assist device implantation in a young patient with non-compaction cardiomyopathy and hereditary spherocytosis.
Huenges K, Panholzer B, Cremer J, Haneya A.
Eur J Cardiothorac Surg. 2018;53(4):879-880.
Ventricular assist device implantation in a young patient with non-compaction cardiomyopathy and hereditary spherocytosis.
16731037
 MALE Adult
Non-compaction cardiomyopathy in an adult with hereditary spherocytosis.
Alter P, Maisch B.
Eur J Heart Fail. 2007;9(1):98-9.
Non-compaction cardiomyopathy in an adult with hereditary spherocytosis.
16731037
 MALE Adult
Non-compaction cardiomyopathy in an adult with hereditary spherocytosis.
Alter P, Maisch B.
Eur J Heart Fail. 2007;9(1):98-9.
To our knowledge, combined occurrence of non-compaction cardiomyopathy, skeletal myopathy and hereditary spherocytosis has not previously been reported.