Search results
Results from the WOW.Com Content Network
Distal muscular dystrophy, also called distal myopathy, is essentially any muscle disease that preferentially affects the hands and/or feet, a much less common pattern than proximal muscle weakness. Late adult-onset type 1; Late adult-onset type 2a; Late adult-onset type 2b; Early adult-onset type 1; Early adult-onset type 2; Early adult-onset ...
This category contains disorders of the muscular system This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision . Generally, diseases outlined within the ICD-10 codes M60-M63 within Chapter XIII: Diseases of the musculoskeletal system and connective tissue should ...
This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes G70-G73 within Chapter VI: Diseases of the nervous system should be included in this category.
Muscular dystrophies (MD) are a genetically and clinically heterogeneous group of rare neuromuscular diseases that cause progressive weakness and breakdown of skeletal muscles over time. [1] The disorders differ as to which muscles are primarily affected, the degree of weakness, how fast they worsen, and when symptoms begin. [ 1 ]
Muscular dystrophies, including Duchenne's and Becker's, are a large group of diseases, many of them hereditary or resulting from genetic mutations, where the muscle integrity is disrupted, they lead to progressive loss of strength and decreased life span. [17] Further causes of neuromuscular diseases are: Polymyositis. Inflammatory muscle ...
This is a list of major and frequently observed neurological disorders (e.g., Alzheimer's disease), symptoms (e.g., back pain), signs (e.g., aphasia) and syndromes (e.g., Aicardi syndrome). There is disagreement over the definitions and criteria used to delineate various disorders and whether some of these conditions should be classified as ...
This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes M00-M99 within Chapter XIII: Diseases of the musculoskeletal system and connective tissue should be included in this category.
Muscular dystrophy congenital infantile cataract hypogonadism; Muscular dystrophy congenital, merosin negative; Muscular dystrophy, facioscapulohumeral; Muscular dystrophy Hutterite type; Muscular dystrophy limb girdle type 2A, Erb type; Muscular dystrophy limb-girdle autosomal dominant; Muscular dystrophy limb-girdle type 2B, Myoshi type