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High-Dose Beta-Blocker Hypertrophic Cardiomyopathy Therapy in a Patient with Friedreich Ataxia

✍ Scribed by J. Kosutic; D. Zamurovic


Publisher
Springer
Year
2005
Tongue
English
Weight
692 KB
Volume
26
Category
Article
ISSN
0172-0643

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Friedreich Ataxia (FA) is a neurodegenerative disorder characterised by progressive gait disturbance, dysarthria, dysmetria and other coordination disorders. The genetic defect is represented by an expansion of GAA repeats in the frataxin gene (FRDA or X25). Hypertrophic cardiomyopathy is a common f