Summary
A case of an adult polysaccharide myopathy is reported in a patient with progressive muscular atrophy and weakness of limb girdles. Histochemistry and electron microscopy showed in some muscle fibers, a storage material composed of amylopectin-like filaments. Biochemical results were normal and no enzyme deficiency was found. This case is compared with three other published cases. Pathological conditons with amylopectin or amylopectin-like storage material are reviewed.
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© 1981 Springer-Verlag
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Pellissier, J.F., de Barsy, T., Bille, J., Serratrice, G., Toga, M. (1981). Polysaccharide (Amylopectin-like) Storage Myopathy Histochemical, Ultrastructural and Biochemical Studies. In: Jellinger, K., Gullotta, F., Mossakowski, M. (eds) Experimental and Clinical Neuropathology. Acta Neuropathologica Supplementum, vol 7. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-81553-9_84
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DOI: https://doi.org/10.1007/978-3-642-81553-9_84
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-540-10449-0
Online ISBN: 978-3-642-81553-9
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