Abstract
The purpose of this study was to review electrocardiographic (ECG) and vectorcardiographic (VCG) observations in 32 patients with Fabry's disease diagnosed for hemizygosity and heterozygosity for Fabry's disease by physical examination, corneal changes, skin biopsy and biochemical studies, i.e., trihexosyl ceramide concentration in plasma, urinary sediment, and α-galactosidase activity in plasma, leukocytes and tears. ECGs were performed in all patients and VCGs in 15. 13 patients had repeated ECGs.
Original language | English (US) |
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Pages (from-to) | 220-222 |
Number of pages | 3 |
Journal | Advances in Cardiology |
Volume | Vol. 21 |
State | Published - Jan 1 1977 |