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 ]
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.
There is a growing consensus that psychosocial factors are another cause of some MSDs. [11] Some theories for this causal relationship found by many researchers include increased muscle tension, increased blood and fluid pressure, reduction of growth functions, pain sensitivity reduction, pupil dilation, body remaining at heightened state of sensitivity.
One hypothesis suggests that the inflammation-immune reaction, caused by an unknown trigger – likely an undiscovered virus or an autoimmune disorder – is the primary cause of sIBM and that the degeneration of muscle fibers and protein abnormalities are secondary features. [19]
Muscle-eye-brain syndrome; Muscular atrophy ataxia retinitis pigmentosa diabetes mellitus; 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