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Diagnosis of muscular glycogenosis by in vivo natural abundance 13C NMR spectroscopy.
Jehenson, P; Duboc, D; Bloch, G; Fardeau, M; Syrota, A.
Afiliación
  • Jehenson P; Service Hospitalier Frederic Joliot, CEA, Orsay, France.
Neuromuscul Disord ; 1(2): 99-101, 1991.
Article en En | MEDLINE | ID: mdl-1822788
ABSTRACT
Natural abundance 13C NMR (nuclear magnetic resonance) spectroscopy was used to distinguish patients suffering from muscle glycogenosis type V (McArdle's disease) from normal subjects by measuring their muscle glycogen content at rest. Proton-decoupled 13C spectra were obtained in 10-15 min from calf muscles at rest. The ratio of the glycogen/creatine signal areas was 12.9 +/- 1.7 in four McArdle's disease patients and 2.0 +/- 0.7 in seven normal subjects. This technique thus allows the non-invasive diagnosis of muscle glycogenosis.
Asunto(s)
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad del Almacenamiento de Glucógeno Tipo V Tipo de estudio: Diagnostic_studies Límite: Adult / Humans / Middle aged Idioma: En Revista: Neuromuscul Disord Asunto de la revista: NEUROLOGIA Año: 1991 Tipo del documento: Article País de afiliación: Francia
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad del Almacenamiento de Glucógeno Tipo V Tipo de estudio: Diagnostic_studies Límite: Adult / Humans / Middle aged Idioma: En Revista: Neuromuscul Disord Asunto de la revista: NEUROLOGIA Año: 1991 Tipo del documento: Article País de afiliación: Francia