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paralýza hyperkaliemická periodická
Record number d020513 Date 06.06.2025 Type M - MESH Topical term paralýza hyperkaliemická periodická Other term English (Pseudonym) Hyperkalemic Periodic Paralysis
English (Pseudonym) Myotonic Periodic Paralysis
English (Pseudonym) Paralysis, Periodic, Hyperkalemic, Familial
Slovak (Pseudonym) paralýza myotonická periodická
Slovak (Pseudonym) paralýza periodická hyperkaliemická familiárna
Slovak (Pseudonym) obrna periodická hyperkaliemická familiárna
Slovak (Pseudonym) obrna myotonická periodická
Slovak (Pseudonym) obrna hyperkaliemická periodická
See also (Later heading) hyperkaliémia
(Skutočné meno) hyperkaliémia
(Skutočné meno) kanál sodíkový, riadený napätím, typ Nav1.4
(Later heading) kanál sodíkový, riadený napätím, typ Nav1.4
UDC C05.651.701.600C10.668.491.650.600C16.320.565.618.711.600C18.452.648.618.711.600 Note 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) 
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Number of the records: 1