Sandbox GGC5: Difference between revisions
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'''Tardive tibial muscular dystrophy:''' | '''Tardive tibial muscular dystrophy:''' | ||
This disease is a late-onset, autosomal dominant distal myopathy. Symptoms are typically muscle weakness and atrophy that are typically confined to the anterior compartment of the lower leg. Clinical onset of this disease usually occur at 35 to 45 years or later. The natural variant of this disease occurs at positions 34306 and 34315. <ref>PMID:12145747</ref> | This disease is a late-onset, autosomal dominant distal myopathy. Symptoms are typically muscle weakness and atrophy that are typically confined to the anterior compartment of the lower leg. Clinical onset of this disease usually occur at 35 to 45 years or later. The natural variant of this disease occurs at positions 34306 and 34315. <ref name="dyst">PMID:12145747</ref> | ||
'''Muscular dystrophy, limb-girdle, autosomal recessive 10:''' | '''Muscular dystrophy, limb-girdle, autosomal recessive 10:''' | ||
This disease is characterized by progressive weakness of the pelvic and shoulder girdle muscles. Muscular dystrophy is an autosomal recessive denerative myopathy that results in severe disability observed within 20 years of its onset. <ref | This disease is characterized by progressive weakness of the pelvic and shoulder girdle muscles. Muscular dystrophy is an autosomal recessive denerative myopathy that results in severe disability observed within 20 years of its onset. <ref name="dyst" /> | ||
'''Salih myopathy:''' | '''Salih myopathy:''' | ||
