Familial focal loss of cross striations
- 1 January 1977
- journal article
- case report
- Published by Springer Nature in Zeitschrift für Neurologie
- Vol. 216 (3) , 163-172
- https://doi.org/10.1007/bf00313617
Abstract
Summary Two patients, a brother and sister, both suffering from congenital generalized muscle weakness with a progressive course are reported. Muscle biopsy revealed areas with loss of cross striations in the muscle fibers, electronmicroscopically presenting complete disorganization of the myofibrils with streaming of the Z discs and absence of mitochondria. Vesicular nuclei with prominent nucleoli were present in these areas. There was a type I fiber prodominance in both cases. The mean diameter of the type I muscle fibers in one of the cases was too small. Motor endplate alterations in this patient gave no evidence of denervation but were suggestive of a delayed development of motor nerves.Keywords
This publication has 13 references indexed in Scilit:
- Incidence of Z band streaming and myofibrillar disruptions in skeletal muscle from healthy young peopleNeurology, 1976
- Hypotrophic Type I Muscle Fibres with Central Nuclei, and Central Myofibrillar Lysis Preferentially Involving Type II FibresEuropean Neurology, 1974
- Terminal Innervation Ratio in Neuromuscular DiseaseArchives of Neurology, 1973
- Terminal Innervation Ratio in Neuromuscular DiseaseArchives of Neurology, 1973
- Familial myopathy with probable lysis of myofibrils in type I fibersNeurology, 1971
- Neuromuscular disease with type I fiber atrophy, central nuclei, and myotube‐like structuresNeurology, 1969
- The histographic analysis of human muscle biopsies with regard to fiber typesNeurology, 1969
- AN ELECTRON MICROSCOPIC STUDY OF TARGET FIBERS, TARGET—LIKE FIBERS AND RELATED ABNORMALITIES IN HUMAN MUSCLEJournal of Neuropathology and Experimental Neurology, 1969
- Muscle Biopsies in Neuromuscular DiseasesPediatric Clinics of North America, 1967
- [A case of amyotonia congenita characterized by a histological and histochemical anomalie of the neuromuscular junction].1954