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From exercise intolerance to functional improvement: the second wind phenomenon in the identification of McArdle disease.
Scalco, Renata Siciliani; Chatfield, Sherryl; Godfrey, Richard; Pattni, Jatin; Ellerton, Charlotte; Beggs, Andrea; Brady, Stefen; Wakelin, Andrew; Holton, Janice L; Quinlivan, Ros.
Afiliación
  • Scalco RS; MRC Centre for Neuromuscular Diseases and Division of Neuropathology, University College London Institute of Neurology, Queen Square, London, United Kingdom.
  • Chatfield S; MRC Centre for Neuromuscular Diseases and Division of Neuropathology, University College London Institute of Neurology, Queen Square, London, United Kingdom.
  • Godfrey R; MRC Centre for Neuromuscular Diseases and Division of Neuropathology, University College London Institute of Neurology, Queen Square, London, United Kingdom.
  • Pattni J; MRC Centre for Neuromuscular Diseases and Division of Neuropathology, University College London Institute of Neurology, Queen Square, London, United Kingdom.
  • Ellerton C; MRC Centre for Neuromuscular Diseases and Division of Neuropathology, University College London Institute of Neurology, Queen Square, London, United Kingdom.
  • Beggs A; MRC Centre for Neuromuscular Diseases and Division of Neuropathology, University College London Institute of Neurology, Queen Square, London, United Kingdom.
  • Brady S; MRC Centre for Neuromuscular Diseases and Division of Neuropathology, University College London Institute of Neurology, Queen Square, London, United Kingdom.
  • Wakelin A; The Association for Glycogen Storage Disease, United Kingdom.
  • Holton JL; MRC Centre for Neuromuscular Diseases and Division of Neuropathology, University College London Institute of Neurology, Queen Square, London, United Kingdom.
  • Quinlivan R; MRC Centre for Neuromuscular Diseases and Division of Neuropathology, University College London Institute of Neurology, Queen Square, London, United Kingdom.
Arq Neuropsiquiatr ; 72(7): 538-41, 2014 Jul.
Article en En | MEDLINE | ID: mdl-25054987
ABSTRACT
McArdle disease is the most common of the glycogen storage diseases. Onset of symptoms is usually in childhood with muscle pain and restricted exercise capacity. Signs and symptoms are often ignored in children or put down to 'growing pains' and thus diagnosis is often delayed. Misdiagnosis is not uncommon because several other conditions such as muscular dystrophy and muscle channelopathies can manifest with similar symptoms. A simple exercise test performed in the clinic can however help to identify patients by revealing the second wind phenomenon which is pathognomonic of the condition. Here a patient is reported illustrating the value of using a simple 12 minute walk test.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad del Almacenamiento de Glucógeno Tipo V / Prueba de Esfuerzo Tipo de estudio: Clinical_trials / Diagnostic_studies / Prognostic_studies Límite: Humans / Male / Middle aged Idioma: En Revista: Arq Neuropsiquiatr Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad del Almacenamiento de Glucógeno Tipo V / Prueba de Esfuerzo Tipo de estudio: Clinical_trials / Diagnostic_studies / Prognostic_studies Límite: Humans / Male / Middle aged Idioma: En Revista: Arq Neuropsiquiatr Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido