Neuromuscular Disorders
Congenital muscular dystrophies
Feb. 08, 2022
Muscle biopsy in myofibrillar myopathy (1)
Many fibers contain abnormal amorphous material (arrows) and vacuoles. Modified Gomori trichrome stain. (Contributed by Dr. Andrew Waclawik.)
Related
Media
Associated
Disorders
- Becker muscular dystrophy
- CIDP
- Charcot-Marie-Tooth disease
- Duchenne muscular dystrophy
- Kearns-Sayre syndrome
- Kugelberg-Welander disease
- MELAS
- MERRF
- McArdle disease
- Miyoshi distal myopathy
- NARP
- Nonaka distal myopathy
- Stormorken syndrome
- Welander distal myopathy
- Werdnig-Hoffman disease
- acid maltase deficiency
- amyloidosis
- carnitine palmitoyltransferase deficiency
- central core disease
- centronuclear myopathy
- congenital fiber-type disproportion
- cysticercosis
- denervation atrophy
- dermatomyositis
- facioscapulohumeral muscular dystrophy
- hereditary neuropathy with pressure palsy
- inclusion-body myositis
- leprous neuropathy
- limb-girdle muscular dystrophy
- myotubular myopathy
- nemaline rod myopathy
- peripheral nerve vasculitis
- polymyositis
- progressive external ophthalmoplegia
- sarcoid myopathy
- sarcoid neuropathy
- spinal muscular atrophy
- toxoplasmosis
- trichinellosis
- tubular aggregates myopathy