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Neuromuscular Disorders |
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include a variety of disorders, such as muscular dystrophy, multiple sclerosis, and ataxia, that result in degeneration and atrophy of muscle or nerve tissues.
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From the WEST scientific·clinical |
From the EAST traditional·alternative |
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Neuromuscular Disorders Other1-2 of 16 more...
Congenital Myasthenia Information Page
... Congenital myasthenia is an inherited disorder that affects the transmission of signals to the muscles. It results from a variety of genetic defects at the molecules associated with neuromuscular tran...
Source: National Institute of Neurological Disorders and Stroke
Congenital Myopathy Information Page ... Congenital myopathy is a term for any muscle disorder present at birth. By this definition the congenital myopathies could include hundreds of distinct neuromuscular syndromes and disorders. In genera...
Source: National Institute of Neurological Disorders and Stroke
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Neuromuscular Disorders Articles
- Congenital Myasthenia Information Page
... Congenital myasthenia is an inherited disorder that affects the transmission of signals to the muscles. It results from a variety of genetic defects at the molecules associated with neuromuscular tran... - Congenital Myopathy Information Page
... Congenital myopathy is a term for any muscle disorder present at birth. By this definition the congenital myopathies could include hundreds of distinct neuromuscular syndromes and disorders. In genera... - Hereditary Spastic Paraplegia Information Page
... Hereditary spastic paraplegia (HSP), also called familial spastic paraparesis (FSP), refers to a group of inherited disorders that are characterized by progressive weakness and stiffness of the legs. ... - Infantile-onset ascending hereditary spastic paralysis
... Infantile-onset ascending hereditary spastic paralysis is a rare disorder characterized by the progressive weakness and stiffness of arm, leg, and facial muscles. Symptoms of infantile-onset ascending... - Isaac's Syndrome Information Page
... Isaac's syndrome (also known as neuromyotonia, Isaac's-Merten's syndrome, continuous muscle fiber activity syndrome, and quantal squander syndrome) is a rare neuromuscular disorder caused ... - Juvenile primary lateral sclerosis
... Juvenile primary lateral sclerosis is a rare disorder characterized by the progressive weakness and stiffness in arm, leg, and facial muscles. Symptoms of juvenile primary lateral sclerosis begin in e... - Kearns-Sayre Syndrome Information Page
... Kearns-Sayre syndrome (KSS) is a rare neuromuscular disorder with onset usually before the age of 20. It is the result of abnormalities in the DNA of mitochondria - small rod-like structures found in ... - Mitochondrial Myopathies Information Page
... Mitochondrial myopathies are a group of neuromuscular diseases caused by damage to the mitochondria-small, energy-producing structures found in every cell in the body that serve as the cells' "pow... - Myotonia Congenita Information Page
... Myotonia congenita is a genetic, neuromuscular disorder characterized by the slow relaxation of the muscles. Symptoms may include muscle stiffness and hypertrophy (enlargement). The disorder is caused... - Myotonia Information Page
... Myotonia is a neuromuscular disorder characterized by the slow relaxation of the muscles after voluntary contraction or electrical stimulation. Generally, repeated effort is needed to relax the muscle...
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