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Differential Diagnosis For EMG/Abnormal findings


List of current finding(s):

Trauma Causes
Traumatic peripheral neuropathy
High cord injury
Spinal cord transection/traumatic
Fukuyama muscular dystrophy
Infectious Disorders (Specific Agent)
Post-Poliomyelitis syndrome
Poliomyelitis, paralytic, spinal
Poliomyelitis, paralytic, bulbar
Vaccine associated paralytic polio
Poliomyelitis, acute
Viral Myopathy
Infected organ, Abscesses
Myositis, inclusion body
Neoplastic Disorders
Metastasis to spinal cord
Carcinomatous myopathy syndrome
Opsoclonic-myoclonic/paraneoplastic syn
Paraneoplastic myelitis/ANS neuropathy syndrome
Allergic, Collagen, Auto-Immune Disorders
Guillain-Barre syndrome
Dermatomyositis/childhood type
Eaton-Lambert syndrome
Mixed connective tissue disease (MCTD)/Undifferentiated
Isaacs potassium channel myopathy syndrome
Myositis synthetase syndrome/Anti-Jo-1 syndrome
Metabolic, Storage Disorders
Diabetic amyotrophy syndrome
Infantile mitochondrial myopathy/Cox defect
Congenital, Developmental Disorders
Paralysis, upper brachial plexus/Erb
Amyotonia, congenita
Merosin Deficient Muscular Dystrophy
Slow Channel Myasthenic Syndrome
Hereditary, Familial, Genetic Disorders
Duchenne's Muscular Dystrophy/Pseudohypertrophic
Erb's Muscular Dystrophy/Limb Girdle MD
Muscular dystrophy
Muscular dystrophy, limb girdle type
Muscular dystrophy, progressive
Spinal muscle atrophy
Spinal muscle atrophy, infantile
Juvenile spinal muscle atrophy (Kugelberg-Welander)
Kennedy Muscular atrophy disease
Mitochondrial myopathy/MERRF
Myhre Syndrome
Potassium-Aggravated Myotonia
Distal muscular dystrophy (Gowers)
Facioscapulohumeral muscular dystrophy
Kearns-Sayre Ophthalmoplegic Syndrome
Muscular atrophy, infantile, spinal
Myotonia atrophica (Steinert's disease)
Myotonia congenita (Thomsens d.)
Nemaline myopathy
Oculopharyngeal muscular dystrophy
Progressive spinal muscular atrophy
Spinal muscle atrophy/adult type IV
Congenital Muscular Dystrophy
Emery-Dreifuss Muscular Dystrophy/Limb Girdle type
Muscular Dystrophy, Oculogastrointestinal type
Myopathy, Myotubular/Centronuclear
Welander syndrome (See Kugelberg Welander)
Usage, Degenerative, Necrosis, Age Related Disorders
Muscle atrophy
Amyotrophic lateral sclerosis
Primary lateral sclerosis
Progressive bulbar palsy (Duchenne)
Batten-Turner Muscular dystrophy
Pelvifemoral musc. dyst.(Leyden-Moeb.)
Anatomic, Foreign Body, Structural Disorders
Spinal cord compression
Suprascapular Nerve Entrapment
Arteriosclerotic, Vascular, Venous Disorders
Spinal cord infarction
Vegetative, Autonomic, Endocrine Disorders
Hypothyroidism (myxedema)
Myasthenic crisis
Myasthenia gravis
Myasthenic syndrome (Pseudomyasthenia)
Neonatal myasthenia
Reference to Organ System
Motor peripheral neuropathy
Neuromuscular disturbances/disorders
Spinal cord lesion
Motor neuron disease
Radicular neuropathy
Peripheral neuropathy syndrome
Monomelic Amyotrophy
Idiopathic, Unclassified Disorders
Stiff-man syndrome
Motor denervation pathophysiology
Heirarchical Major Groups
Muscle disorders
Steroid myopathy
Drug induced Myopathy
Poisoning (Specific Agent)
Alcohol myopathy
Organ Poisoning (Intoxication)
Drug induced Neuromuscular junct/block.
Abnormal, ELECTROMYOGR, Electromyogram, Electromyographies, Electromyography, Electromyography (EMG), Electromyography (procedure), Electromyography (regime/therapy), EM-Electromyography, EMG, EMG (Electrophysiology), EMG Electromyography
External Links Related to EMG/Abnormal findings
PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)