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Key words: Fabry disease; glomerular proteinuria; lipid involvement, and the third phase involves vascular,storage diseases; hereditary kidney diseases; glyco- cardiac, and cerebral disease and renal functionalsphingolipids; alpha-galactosidase A; angiokeratomas; deterioration.acroparaesthesias; corneal opacities Death occurs around the fifth decade from renal,cardiac, and cerebral complications. Nevertheless, clin-ical evidence supports phenotypic heterogeneity ofFabry’s disease, and genetic heterogeneity has been
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Meroni et al. (1997) studied this question.
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