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Fine Structure of the Human Skeletal Muscle in Myopathy
Tetsuji Santa, MD
Arch Neurol. 1969;20(5):479-489.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings. |
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RECENTLY, progressive muscular dystrophies and other types af myopathies1-6 have been attracting interest in biochemical, physiologic, and morphologic studies. Although the pathogenesis has not been elucidated, study of the nature of myopathies has been accelerated with current electron microscopic techniques.7-10
In 1960, Van Breemen9 reported that early vacuolation of the sarcoplasmic reticulum (SR) was seen as the primary lesion of muscular dystrophy in both light and electron microscopic studies. Platzer and Chase11 examined muscle of dystrophic mice and found alterations in the muscle fiber, especially disappearance of the sarcolemma, which were observed before clinical manifestations. They concluded that the initial defect might involve the sarcolemma. Fisher et al12 described mitochondrial changes as the earliest defect. Ultrastructural studies have also revealed new diseases, such as central core disease,13 myotubular myopathy,14 and megaconial myopathy.15,16 Ultrastructural observations in McArdles disease17 and familial hypokalemic
. . . [Full Text PDF of this Article]
Author Affiliations
Fukuoka, Japan
From the Second Department of Anatomy and the Department of Neurology, Kyushu University, Fukuoka, Japan.
Footnotes
Submitted for publication Feb 27, 1968; accepted Oct 23.
Presented in part at the 23rd scientific meeting of the Japanese Society of Electron Microscopy, Fukuoka, Japan, May 1967.
Reprint requests to Department of Neurology, Neurological Institute, Kyushu University, Fukuoka, Japan.
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