مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Information Journal Paper

Title

LYSOSOMAL MYOPATHIES

Pages

  11-11

Abstract

 Lysosomal myopathies are hereditary myopathies characterized morphologically by the presence of autophagic vacuoles. Autophagy is an intracellular bulk degradation process, which is used by all cells to eliminate waste materials. Autophagy is considered to be essential for myocytes and the lysosomal system becomes prominent in certain muscle diseases.In muscle pathology, lysosomal abnormalities are seen in three types of vacuoles: rimmed vacuoles which are most likely a secondarily induced lysosomal abnormality, autophagic vacuoles, which are usually large and contain glycogen, seen specifically in ACID MALTASE DEFICIENCY and autophagic vacuoles with unique sarcolemmal features with acetyl cholinesterase activity (AVSF), which are seen in DANON disease and other related myopathies.

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    • Cite

    APA: Copy

    NILIPOUR, YALDA. (2012). LYSOSOMAL MYOPATHIES. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), 6(4 (SUPPL 1)), 11-11. SID. https://sid.ir/paper/303466/en

    Vancouver: Copy

    NILIPOUR YALDA. LYSOSOMAL MYOPATHIES. IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN)[Internet]. 2012;6(4 (SUPPL 1)):11-11. Available from: https://sid.ir/paper/303466/en

    IEEE: Copy

    YALDA NILIPOUR, “LYSOSOMAL MYOPATHIES,” IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), vol. 6, no. 4 (SUPPL 1), pp. 11–11, 2012, [Online]. Available: https://sid.ir/paper/303466/en

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