Die sogenannte congenitale centronucleäre Myopathie —eine primäre Neuropathie?

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ID: 116885
1970
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Abstract
Report of a case with congenital symmetrical slowly progressive neuromuscular disease. EMG shows signs of neurogenic atrophy together with a predominant myopathic pattern. Muscle biopsy reveals the characteristics of so-called centronuclear myopathy in combination with “myotube-like structures”. Myometric studies show preferential atrophy of type-I-fibres. Biopsy of the sural nerve indicates involvement of the peripheral nerve. The question whether this disease is essentially neurogenic or myopathic, is discussed. Neurogenic origin is given preference.
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pongratz1970actadie Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors D. Pongratz;M. Heuser;F. Mittelbach;A. Struppler;D. Pongratz;M. Heuser;F. Mittelbach;A. Struppler;
Journal acta neuropathologica
Year 1970
DOI
doi:10.1007/BF00686063
URL
https://link.springer.com/article/10.1007/BF00686063
Keywords
pathology neurosciences

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