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Brody myopathy demonstrates a pseudo-increment on repetitive nerve stimulation.
Masingue, Marion; Arzel, Marianne; Sternberg, Damien; Stojkovic, Tanya; Behin, Anthony; Bassez, Guillaume; Vicart, Savine; Péréon, Yann; Magot, Armelle; Kuntzer, Thierry; Eymard, Bruno; Fournier, Emmanuel.
Afiliación
  • Masingue M; Reference Center for Neuromuscular Diseases Nord-Est-Ile de France, Institute of Myology, CHU Pitié Salpetrière, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Arzel M; Department of Neurophysiology, CHU Pitié Salpetrière, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Sternberg D; National Reference Center for Muscle Channelopathies, Groupe Hospitalier Pitié Salpetrière, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Stojkovic T; Biochemistry Department, Center of Molecular and Cellular Genetics, Groupe Hospitalier Pitié Salpetrière, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Behin A; Reference Center for Neuromuscular Diseases Nord-Est-Ile de France, Institute of Myology, CHU Pitié Salpetrière, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Bassez G; Reference Center for Neuromuscular Diseases Nord-Est-Ile de France, Institute of Myology, CHU Pitié Salpetrière, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Vicart S; Reference Center for Neuromuscular Diseases Nord-Est-Ile de France, Institute of Myology, CHU Pitié Salpetrière, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Péréon Y; National Reference Center for Muscle Channelopathies, Groupe Hospitalier Pitié Salpetrière, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Magot A; Reference Center for Neuromuscular Diseases Atlantique-Occitanie-Caraïbes, CHU Nantes, Nantes, France.
  • Kuntzer T; Reference Center for Neuromuscular Diseases Atlantique-Occitanie-Caraïbes, CHU Nantes, Nantes, France.
  • Eymard B; Department of Neurology, Lausanne University Hospital CHUV, Lausanne, Switzerland.
  • Fournier E; Reference Center for Neuromuscular Diseases Nord-Est-Ile de France, Institute of Myology, CHU Pitié Salpetrière, Assistance Publique Hôpitaux de Paris, Paris, France.
Muscle Nerve ; 61(4): 491-495, 2020 04.
Article en En | MEDLINE | ID: mdl-31944327
ABSTRACT

INTRODUCTION:

Brody myopathy (BM) is a recessive condition caused by mutations in the ATP2A1 gene and usually induces impaired muscle relaxation during and after exercise. Diagnosis relies on needle electromyography showing electrical silence, muscle biopsy with decreased sarcoplasmic reticulum calcium adenosine triphosphatase activity, and genetic analysis. Electrodiagnostic functional analyses are useful in the diagnosis of channelopathies, and thus may be impaired in BM.

METHODS:

We performed exercise tests and repetitive nerve stimulation (RNS; 10 supramaximal stimuli at 3 Hz) in 10 patients with BM.

RESULTS:

All participants showed incremental responses on RNS. Compound muscle action potential amplitude was increased and duration was decreased, especially in the ulnar nerve (+30.2 ± 7.1% and - 30.3 ± 2.8%, respectively; both P < .001).

DISCUSSION:

Easily accessible, this sign, referred to as the Arzel sign, could prove to be a very useful tool in BM diagnosis and in broadening its phenotype.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Nervio Cubital / Potenciales de Acción / Músculo Esquelético / Electrodiagnóstico / Miotonía Congénita Límite: Female / Humans / Male Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Nervio Cubital / Potenciales de Acción / Músculo Esquelético / Electrodiagnóstico / Miotonía Congénita Límite: Female / Humans / Male Idioma: En Año: 2020 Tipo del documento: Article