Summary. Epidemiology. FSHD is a rare familial disease with an estimated prevalence of 1/20, It is the 3rd most common form of hereditary myopathy. Entre as entidades que compõem o leque da distrofia muscular progressiva . da DMP fácio-escápulo-umeral e da distrofia miotônica (Steinert) (Tabela 6). da incapacidade) da V&A com a idade em algumas doenças, como a distrofia muscular de Duchenne, distrofia fascio-escapulo-umeral, distrofia miotônica.
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Correlation of disability with age and serum enzymes in neuromuscular disorders.
Professor Titular de Neurologia. A negative correlation decrease disability with age was found for multicore myopathy, benign myopathy of childhood with type 1 predominance, ukeral myopathy deficiency and dermatomyositis.
Full text available only in PDF format. Clinical investigation in Duchenne dystrophy: Determination of the power of the therapeutic trials based on the natural history.
Clinical trial in Duchenne dystrophy. The design of the protocol.
Diagnostic and prognostic significance of serum enzymes: Arch Phys Med Rehabil Aids to the examination of the peripheral nervous system. Mendel JR, Florence J.
Clinical trials in neuromuscular disease. Serum enzyme alterations in neuromuscular disorders.
Drug treatment for facioscapulohumeral muscular dystrophy.
Blood enzymes in Duchenne’s progressive muscular dystrophy and their correlation with the clinical and histological pictures. Acta Med Pol Warszawa Arch Neurol4: Specific tests for polymyositis.
The diagnostic value of serum creatinekinase in neuromuscular and muscular disease. Maintenance of ambulation in childhood muscular dystrophy.
OMIM Entry – # – FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1; FSHD1
J Chronic Dis Management of progressive muscular dystrophy of childhood. Serum pyruvate-kinase and creatine-phosphokinase in progressive muscular dystrophies. J Neurol Sci Assessment of muscle strenght in Duchenne muscular dystrophy. All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License. Services on Demand Journal. How to cite this article.