Roger W.BloweyBSc BVSC FRCVS FRAgS,A. DavidWeaverBSc DR MED VET PHD FRCVS, inColor Atlas of Diseases and Disorders of Cattle (Third Edition), 2011 White muscle disease (enzootic muscle dystrophy, “flying scapula”) Definition: muscle degeneration caused byvitamin Eand/orselenium de...
We studied a 29-year-old man with slowly progressive proximal leg weakness, calf hypertrophy, and high serum levels of creatine kinase activity. Clinically, it was not possible to identify his as a sporadic instance of Becker muscular dystrophy (BMD) or one of spinal muscular atrophy. The ...
Clinically, it was not possible to identify his as a sporadic instance of Becker muscular dystrophy (BMD) or one of spinal muscular atrophy. The problem arose because electromyography and elevated creatine kinase suggested a myopathy whereas changes in the muscle biopsy resembled a neurogenic disorder...
Duchenne muscular dystrophy is a severe, progressive, muscle-wasting disease that leads to difficulties with movement and, eventually, to the need for assisted ventilation and premature death. The disease is caused by mutations in DMD (encoding dystrophi
In 14 patients with limb girdle muscular dystrophy, polymyositis, and type 3 spinal muscular atrophy, CT scans of the thigh muscles were correlated with si... MS Schwartz,M Swash,DA Ingram,... - 《Muscle & Nerve》 被引量: 30发表: 2010年 ...
Preclinical testing of potential therapies for Duchenne muscular dystrophy (DMD) is conducted predominantly of the mdx mouse. But lack of a detailed quantitative description of the pathology of this animal limits our ability to evaluate the effectiveness of putative therapies or their relevance to DMD...
Severe degenerative features of the nervous system of a hitherto unknown kind, associated with a neuromuscular disorder with histopathological features of congenital muscular dystrophy, are reported in two female siblings. The clinical profile was characterized by generalized hypotonia followed by spastic ...
Heredofamilial juvenile muscular atrophy simulating muscular dystrophy. AMA Arch Neurol Psych. 1956;75(5):500–9. Article CAS Google Scholar Dubowitz V: Sixty years of spinal muscular atrophy: a personal odyssey. In: Sumner CJ, Paushkin S, Ko C. Spinal muscular atrophy disease mechanisms and...
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominantly inherited muscular dystrophy with late onset (usually after 45 years of age) ptosis, dysphagia, and usually less prominent limb involvement. From: Physical Medicine and Rehabilitation Clinics of North America, 2012 ...
X连锁婴儿脊髓性肌萎缩症的英文名字是Infantile Spinal Muscular Atrophy, X-Linked。基因解码表明:佳学基因通过基因解码发现:X连锁婴儿脊髓性肌萎缩症是由基因突变引起的。这种疾病是由SMN1基因的突变或缺失引起的,该基因编码脊髓性肌萎缩症蛋白(SMN蛋白),该蛋白在神经元中起着重要的功能。SMN蛋白的缺乏会导致神经元...