Neuropathies: These disorders involve damage or dysfunction of the peripheral nerves, which transmit signals between the central nervous system (the brain and spinal cord) and the rest of the body. Neuropathies can be acquired, resulting from factors like trauma, infections, or metabolic issues, or they can be inherited due to genetic mutations.
Myopathies: Myopathies are conditions that mainly affect the muscles themselves. They can be genetic (inherited) or acquired, stemming from causes like inflammation, toxins, or metabolic problems.
Muscular Dystrophies: This group comprises genetic disorders characterized by progressive muscle weakening and degeneration. They occur due to mutations in genes responsible for producing proteins crucial for muscle function.
Neuromuscular Junction Disorders: These disorders entail issues at the point where nerve cells communicate with the muscles they control. Conditions like myasthenia gravis fall under this category.
Motor Neuron Diseases: These disorders affect the nerve cells (motor neurons) in the brain and spinal cord that oversee voluntary muscles. Conditions such as amyotrophic lateral sclerosis (ALS or Lou Gehrig's Disease) and spinal muscular atrophy (SMA) are examples of motor neuron diseases.
Amyotrophic Lateral Sclerosis (ALS, or Lou Gehrig's Disease), Spinal Muscular Atrophies (SMA), and Motor Neuron Disease
Important LinksAutonomic Nervous System Disorders
Brachial and Lumbar Plexopathies
Charcot-Marie-Tooth (CMT) and Other Hereditary Neuropathies
Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
Entrapment Neuropathies (Carpal Tunnel, Ulnar Neuropathy, Peroneal Neuropathy, and Tarsal Tunnel Syndrome)
Guillain-Barré Syndrome
Hereditary and Acquired Ataxias
Hereditary Spastic Paraplegia
Inflammatory Myopathies (Polymyositis, Dermatomyositis, and Inclusion Body Myositis)
Muscular Dystrophies (Facioscapulohumeral (FSH) Dystrophy and Limb-Girdle Dystrophy (LGMD))
Myasthenia Gravis (MG) and Lambert-Eaton (LEMS)
Myopathies (Endocrine, Drug-induced, Metabolic, and Mitochondrial) and Cramping
Myotonic Dystrophy and Myotonic Syndromes
Neuropathies (Diabetic, Drug-induced, Inflammatory, Paraproteinemias
Periodic Paralysis
Post-Polio Syndrome
EMG
Nerve Conduction Studies
Repetitive Stimulation
Evoked Potentials (Somatosensory, Visual, and Acoustic Brain Stem)
Single Fiber Electromyography
Muscle and nerve biopsies
Spinal fluid analysis
Genetic counselling and testing
Unexplained Stiffness
Cramps, contracture, fatigue, exercise intolerance
Pain
Tingling
Numbness
Foot Drop
Limb Weakness