Related MeSH Hierarchy (4)
Diseases [C] » Musculoskeletal Diseases [C05] » Muscular Diseases » Paralyses, Familial Periodic » Paralysis, Hyperkalemic Periodic
Diseases [C] » Nervous System Diseases [C10] » Neuromuscular Diseases » Muscular Diseases » Paralyses, Familial Periodic » Paralysis, Hyperkalemic Periodic
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Metal Metabolism, Inborn Errors » Paralyses, Familial Periodic » Paralysis, Hyperkalemic Periodic
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Metal Metabolism, Inborn Errors » Paralyses, Familial Periodic » Paralysis, Hyperkalemic Periodic
Description
An autosomal dominant familial disorder which presents in infancy or childhood and is characterized by episodes of weakness associated with hyperkalemia. During attacks, muscles of the lower extremities are initially affected, followed by the lower trunk and arms. Episodes last from 15-60 minutes and typically occur after a period of rest following exercise. A defect in skeletal muscle sodium channels has been identified as the cause of this condition. Normokalemic periodic paralysis is a closely related disorder marked by a lack of alterations in potassium levels during attacks of weakness. (Adams et al., Principles of Neurology, 6th ed, p1481) MeSH
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Approved Indicated Drugs (1)
Phase 3 Indicated Drugs (1)
Organization Involved with Phase 3 Indications (5)
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UMLS Data
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