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Background. Fabry Disease is a rare, X-chromosomal inherited lysosomal  storage disease with a consequent intracellular accumulation of neutral  glycosphingolipids in various tissues. This can cause skin and ocular  lessions, progressive renal, cardiac or cerebrovascular disorders. If a  person in a family has Fabry disease, other family members including even  extended relatives, may also be at risk. Case report. We presented three  cases pointed out various manifestation of Fabry disease, that illustrate a  possible cause for otherwise unexplained cardiac hypertrophy and various  rhythm and conduction abnormalities. Conclusion. Although most symptoms begin  in childhood, various manifestations often lead to misdiagnosis and clinical  diagnosis is frequently delayed for many years, even decades. Enzyme  replacement therapy has become available, pointing out the importance of  early diagnosis so that treatment can be initiated before irreversible organ  damage

Fabry disease, do we think enough about this multisystemic disorder?: A presentation of three cases in a Serbian family