Literature DB >> 127507

Malignant hyperthermia in a family. The neurophysiological and light microscopical study of muscle biopsies of healthy members.

E Reske-Nielsen, J Haase, J Kelstrup.   

Abstract

12 healthy persons--close relatives to two children who died of malignant hyperthermia--volunteered for biopsies of striated muscle and skin, electromyography and electroencephalography. The investigations of muscle biopsies comprised material for enzyme histochemistry and ordinary light microscopy including visualization of the intramuscular nerves. Out of 12 clinically healthy persons 9 revealed abnormalities of the muscle fibres, 11 showed degenerative and regenerative alterations in the intramuscular nerves, in EMG 7 turned out to produce slight neuropathy, and 7 displayed abnormal EEG tracings. These findings support the idea that the etiological key (or keys) in the peculiar pathophysiological entity of malignant hyperthermia may even be found outside the striated muscle cell.

Entities:  

Mesh:

Substances:

Year:  1975        PMID: 127507

Source DB:  PubMed          Journal:  Acta Pathol Microbiol Scand A        ISSN: 0365-4184


  2 in total

1.  The adenosine triphosphate (ATP) depletion test: comparison with the caffeine contracture test as a method of diagnosing malignant hyperthermia susceptibility.

Authors:  B A Britt; L Endrenyi; W Kalow; P L Peters
Journal:  Can Anaesth Soc J       Date:  1976-11

2.  Ryanodine receptor 1 (RYR1) mutations in two patients with tubular aggregate myopathy.

Authors:  Gaetano Nicola Alfio Vattemi; Daniela Rossi; Lucia Galli; Maria Rosaria Catallo; Elia Pancheri; Giulia Marchetto; Barbara Cisterna; Manuela Malatesta; Enrico Pierantozzi; Paola Tonin; Vincenzo Sorrentino
Journal:  Eur J Neurosci       Date:  2022-06-13       Impact factor: 3.698

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.