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paralýzy familiárne periodické
Č. záznamu d010245 Dátum 06.06.2025 Typ M - MESH Tematický termín paralýzy familiárne periodické Iný termín Angličtina (Pseudonym) Normokalemic Periodic Paralysis
Angličtina (Pseudonym) Periodic Paralysis, Familial
Slovenčina (Pseudonym) paralýza periodická normokaliemická
Slovenčina (Pseudonym) paralýza familiárna periodická
MDT C05.651.701C10.668.491.650C16.320.565.618.711C18.452.648.618.711 Poznámka A heterogenous group of inherited disorders characterized by recurring attacks of rapidly progressive flaccid paralysis or myotonia. These conditions have in common a mutation of the gene encoding the alpha subunit of the sodium channel in skeletal muscle. They are frequently associated with fluctuations in serum potassium levels. Periodic paralysis may also occur as a non-familial process secondary to THYROTOXICOSIS and other conditions. (From Adams et al., Principles of Neurology, 6th ed, p1481) 
predmetové heslo
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