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paralýzy familiárne periodické
Record number d010245 Date 06.06.2025 Type M - MESH Topical term paralýzy familiárne periodické Other term English (Pseudonym) Normokalemic Periodic Paralysis
English (Pseudonym) Periodic Paralysis, Familial
Slovak (Pseudonym) paralýza periodická normokaliemická
Slovak (Pseudonym) paralýza familiárna periodická
UDC C05.651.701C10.668.491.650C16.320.565.618.711C18.452.648.618.711 Note 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) 
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