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. 2006 Aug 16;95(11):569–583. doi: 10.1007/s00392-006-0427-2

Table 1.

Myocardial storage diseases

Amyloidosis
Lysosomal storage disease (e.g., morbus Gaucher)
Glycogen storage disease (e.g., morbus Pompe)
Glycosphingolipid storage disease (morbus Fabry)
Mucopolysaccharidosis (e.g., morbus Hurler)
Hemochromatosis