Esta protei slideshare uses cookies to improve functionality and performance, and to provide you with relevant advertising. Distrofia muscular congenita las enfermedades raras. Duchenne muscular dystrophy is an xlink recessive disorder that affects 1 per 3. Sep 01, 2014 sindrome del piramidal o falsa ciatica. Al tener informacion correcta sobre nuestra enfermedad, podemos monitorear y proteger nuestra salud en buena medida. Duchennebecker muscular dystrophies are diagnosed by immunohistochemistry, western blot andor dna analysis. Atrofia muscular progresiva sintomas, causas, medicamentos, diagnostico, y diagnosticos erroneos. Overview of muscular dystrophies beyond the basics. Clinical features and diagnosis of duchenne and becker muscular distrophy. Atrofia muscular espinal genetic and rare diseases. Both diseases are the result of a mutation in the xp21 gene that encodes for dystrophin. Distrofia y ejercicio ejercicio aerobico musculo prueba. Facioscapulohumeral muscular dystrophy is the third most common muscular dystrophy with an estimated prevalence of 1 per 20.
Atrofia muscular progresiva binipatia e higienismo. Genic and cellular therapy are yet on experimental field. Hipertrofia muscular e nutricao repositorio aberto. Becker muscular dystrophy is less common, affecting approximately 1 per 30 000 males. Treatment of muscular dystrophies is based in physiotherapy, ventilatory support, surgery and drugs mainly esteroids, effective in duchennebecker muscular dystrophies.
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