Distal myopathy
MONDO:0018949Distal myopathy refers to a group of muscle diseases which share the clinical pattern of predominant weakness and atrophy beginning in the feet and/or hands.
Also known as: distal muscular dystrophy, distal myopathy, Miyoshi muscular dystrophy
40 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Myopathy, distal, 5
(1)
Adult-onset distal myopathy due to VCP mutation
(0)
Asymetric thumb-handgrip weakness-distal myopathy
(0)
Asymptomatic hyperckemia-myalgia-rhabdomyolysis syndrome
(0)
Autosomal dominant distal myopathy
(0)
Calf-predominant weakness-gastrocnemius medialis atrophy-distal myopathy
(0)
Distal myopathy, Tateyama type
(0)
Distal myopathy, Welander type
(0)
Distal myopathy with anterior tibial onset
(0)
Distal myopathy with posterior leg and anterior hand involvement
(0)
Distal myopathy with vocal cord weakness
(0)
Finnish upper limb-onset distal myopathy
(0)
KLHL9-related early-onset distal myopathy
(0)
Miyoshi muscular dystrophy 1
(0)
Miyoshi muscular dystrophy 2
(0)
Miyoshi muscular dystrophy 3
(0)
Miyoshi myopathy
(0)
MYH7-related skeletal myopathy
(0)
Myofibrillar myopathy 2
(0)
Myofibrillar myopathy 3
(0)