Muscular Dystrophies include a heterogeneous series of diseases
that range from childhood to adult onset cases, of difficult
diagnosis and treatment. This book presents the state of the art in
muscular dystrophies, after the molecular revolution. In the field
of patients' diagnosis, several advances have been done by
recognising new entities. New techniques such as biochemical,
molecular advancements, and the use of muscle MRI are collected
that allow rapid diagnosis. Also, advances in therapy and
therapeutical trials are presented in Duchenne and other muscular
dystrophies and some novel treatments in glycogen storage disease
by enzyme replacement are proposed. Both rehabilitation techniques
and other treatments deserve particular attention for the
improvements observed.
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