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Dystrophin detection by immunofluorescent technique for diagnosing muscular dystrophy / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 239-242, 2002.
Artículo en Chino | WPRIM | ID: wpr-245324
ABSTRACT
<p><b>OBJECTIVE</b>To establish a specific technique for diagnosing and classifying Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), facioscapulohumeral muscular dystrophy (FSHD) and neurologic dystrophy.</p><p><b>METHODS</b>Forty-seven cases were detected by immunofluorescence technique for analyzing dystrophin located in skeletal muscle cell membrane with the use of mouse monoclonal antibodies, goat and rabbit polyclonal antibodies.</p><p><b>RESULTS</b>The normal individuals showed ringed positive staining stripe around muscle fibers. Negative result of staining was seen in 16 DMD patients. Eleven BMD patients had discontinuous or a patchy positive staining pattern, and all of 10 FSHD and 10 neurological amyotrophic patients showed positive dystrophin staining.</p><p><b>CONCLUSION</b>Detecting dystrophin in the skeletal muscle cell membrane of muscular patients is an efficient technique for diagnosing and classifying various types of muscular dystrophy.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Patología / Química / Distrofina / Técnica del Anticuerpo Fluorescente / Músculo Esquelético / Distrofia Muscular de Duchenne / Distrofia Muscular Facioescapulohumeral / Diagnóstico / Diagnóstico Diferencial / Metabolismo Tipo de estudio: Estudio diagnóstico Límite: Adolescente / Adulto / Niño / Child, preschool / Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2002 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Patología / Química / Distrofina / Técnica del Anticuerpo Fluorescente / Músculo Esquelético / Distrofia Muscular de Duchenne / Distrofia Muscular Facioescapulohumeral / Diagnóstico / Diagnóstico Diferencial / Metabolismo Tipo de estudio: Estudio diagnóstico Límite: Adolescente / Adulto / Niño / Child, preschool / Femenino / Humanos / Masculino Idioma: Chino Revista: Chinese Journal of Medical Genetics Año: 2002 Tipo del documento: Artículo