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Isolated cardiac manifestations in Fabry disease: the UK experience

✍ Scribed by B Sachdev; PM Elliott

Book ID
114813301
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
122 KB
Volume
91
Category
Article
ISSN
0803-5253

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## Background: Fabry disease results from a genetic deficiency of alpha-galactosidase a (gla) activity. phenotype-genotype correlations in this condition have not as yet been fully elucidated. ## Objective: To report a case of a male patient with classical fabry disease and his mother, a heterozy