The literature concerning muscle Glycogenoses reflects a worldwide
interest which has been greatly intensified, mainly over the last
ten years. To a large extent, this renewed interest is due to
recent advances in diagnosing and treating the Lysosomal disease
named Glycogenosis II or Pompe disease (GSD II). The new
therapeutic approaches must induce us to make a great effort in
order to better diagnose, treat and follow correctly the patients
with Pompe disease. This book is a comprehensive text which covers
all of the aspects regarding this disease, from pathogenic to
clinical and therapeutic features. (Imprint: Nova Biomedical).
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