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Myopathy (Pattern Recognition) - Coggle Diagram
Myopathy (Pattern Recognition)
Distal
Late-onset
Type I (Welander)
Type II (LGMD2A, LGMD2B)
Early-onset
Type I (Nonaka)
Type II (Miyoshi)
Type III (Laing)
Mixed
Proximal arms + Distal legs
Facioscapulohumeral Dystrophy (FSHD)
Emery-Dreifuss MD
Pompe disease (acid maltase deficiency)
Congenital Scapuloperoneal Syndrome
Limb-Girdle MD (LGMD)
LGMD2A (Calpainopathy)
LGMD2C-F (Sarcoglycanopathy)
LGMD2I (FKRP)
Nemaline myopathy
Central core myopathy
Distal arms + Proximal legs
Inclusion Body Myositis (IBM)
Myotonic Dystrophy
Proximal
Ptosis
With Ophthalmoparesis
Oculopharyngeal MD
Oculopharyngodistal Myopathy
Mitochondrial
Congenital
Centronuclear, Multicore
Without Ophthalmoparesis
Myotonic Dystrophy
Congenital
Central core, Myofibrillary, Nemaline
Neck extensor weakness
Isolated neck extensor myopathy
Autoimmune
Dermatomyositis/Polymyositis
Congenital myopathy
Endocrine
Hyperparathyroidism
Bulbar weakness
Oculopharyngeal MD
Episodic weakness/ rhabdomyolysis
Exercise-related
Glycogen storage
McArdle disease
Lipid disorder
Carnitine palmitotransferase deficiency
Not exercise-related
Toxic/Drug-induced
Malignant hyperthermia
Central core myopathy
Duchenne MD
Autoimmune (Polymyositis/Dermatomyositis) - rare
Infective (viral/bacterial)
Central (non-muscular)
Neuroleptic malignant syndrome (NMS)
Status epilepticus
Stiffness
Hyperkalaemic Periodic Paralysis
Hypothyroidism
Myotonia congenita
Paramyotonia congenita
Cardiac disease
Arrhythmia
Andersen-Tawil syndrome
Kearns-Sayre syndrome
Polymyositis
Muscular dystrophies
LGMD1B, 2C-F, 2G, Emery-Dreifuss
Congestive Heart Failure
Muscular dystrophies
Duchenne, Becker, Emery-Dreifuss, Myotonic, LGMD1B, 2C-F, 2G
Nemaline
Metabolic (Pompe disease, Carnitine deficiency)
Polymyositis
Contracture
Brody disease
Glycogen storage disorder
Hypothyroidism
Paramyotonia congenita
Rippling muscle disease
Respiratory insufficiency
Muscular dystrophy (Becker, Duchenne, Emery-Dreifuss, LGMD2A, 2I, Myotonic)
Metabolic (Glycogen storage/Lipid disorders)
Mitochondrial
Congenital (Centronuclear, Nemaline)
Autoimmune (Polymyositis)