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Up to: Congenital myopathy
Congenital structural myopathy
A group of rare genetic muscle disorders characterized by hypotonia, muscle weakness, and delayed development of motor skills.
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Inborn mitochondrial myopathy 18 trials · 45 incl. sub-types Sub-types →
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Nemaline myopathy 13 trials Sub-types →
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Myofibrillar myopathy 1 trial · 3 incl. sub-types Sub-types →