Anderson Fabry's disease (AFD) is a rare but underdiagnosed intracellular lipid disorder which can cause left ventricular hypertrophy (LVH). Pre-clinical diagnosis of Fabry's disease is important as it permits early stratification for enzyme replacement therapy, improving the patient's long-term prognosis, avoiding progression to irreversible fibrosis, and preventing cardiovascular complications.Combinations of imagingmodalities that integrate the strengths of each modality and at the same time eliminate weaknesses of an individual modality can offer improved diagnostics, therapeutic monitoring, and pre-clinical assessment of Fabry's disease. This reviewdiscusses the advantages and challenges in developingmultimodality imaging systems of Fabry's cardiomyopathy, highlights somesuccessful combinations that are nowroutinely used in the clinic and in research, and discusses recent advances in multimodality instrumentation that may offer new opportunities for pre-clinical assessment of this disease.

Multimodality imaging for pre-clinical assessment of Fabry's cardiomyopathy

Madonna R.;
2014-01-01

Abstract

Anderson Fabry's disease (AFD) is a rare but underdiagnosed intracellular lipid disorder which can cause left ventricular hypertrophy (LVH). Pre-clinical diagnosis of Fabry's disease is important as it permits early stratification for enzyme replacement therapy, improving the patient's long-term prognosis, avoiding progression to irreversible fibrosis, and preventing cardiovascular complications.Combinations of imagingmodalities that integrate the strengths of each modality and at the same time eliminate weaknesses of an individual modality can offer improved diagnostics, therapeutic monitoring, and pre-clinical assessment of Fabry's disease. This reviewdiscusses the advantages and challenges in developingmultimodality imaging systems of Fabry's cardiomyopathy, highlights somesuccessful combinations that are nowroutinely used in the clinic and in research, and discusses recent advances in multimodality instrumentation that may offer new opportunities for pre-clinical assessment of this disease.
2014
Madonna, R.; Cevik, C.; Cocco, N.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1021820
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