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Distal Myopathies

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Definition: A heterogeneous group of genetic disorders characterized by progressive MUSCULAR ATROPHY and MUSCLE WEAKNESS beginning in the hands, the legs, or the feet. Most are adult-onset autosomal dominant forms. Others are autosomal recessive.      Other names Udd Markesbery Muscular Dystrophy; Myopathy, Distal; Myopathies, Distal; Muscular Dystrophy, Udd-Markesbery; Muscular Dystrophy, Tibial; Muscular Dystrophy, Finnish-Markesbery; Muscular Dystrophies, Distal; Finnish Markesbery Muscular Dystrophy; Distal Myopathy, Welander; Distal Muscular Dystrophy; Welander Distal Myopathy; Udd-Markesbery Muscular Dystrophy; Tibial Muscular Dystrophy; Finnish-Markesbery Muscular Dystrophy; Distal Myopathy; Distal Muscular Dystrophies; Muscular Dystrophy, Distal
 
SubstanceCAS Registry & nameCategoriesSource
Jankovic Rivera syndrome  0   *Distal Myopathies.
Miyoshi myopathy  0   *Muscular Atrophy *Distal Myopathies.
Distal myopathy, Nonaka type  0   *Distal Myopathies.
Distal myopathy Markesbery-Griggs type  0   *Distal Myopathies.
Welander distal myopathy, Swedish type  0   *Distal Myopathies.

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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