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Polysaccharide (Amylopectin-like) Storage Myopathy Histochemical, Ultrastructural and Biochemical Studies

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Experimental and Clinical Neuropathology

Part of the book series: Acta Neuropathologica Supplementum ((NEUROPATHOLOGIC,volume 7))

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

  • eBook Packages: Springer Book Archive

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