Hyperkalemic periodic paralysis with cardiac dysrhythmia: a novel sodium channel mutation?

Article Details

Citation

Baquero JL, Ayala RA, Wang J, Curless RG, Feero WG, Hoffman EP, Ebeid MR

Hyperkalemic periodic paralysis with cardiac dysrhythmia: a novel sodium channel mutation?

Ann Neurol. 1995 Mar;37(3):408-11.

PubMed ID
7695243 [ View in PubMed
]
Abstract

A patient is presented with hyperkalemic periodic paralysis (HyperPP) and a cardiac dysrhythmia. An amino acid substitution (Val783Ile) in the adult skeletal muscle sodium channel gene was detected. Although lack of available family members precluded rigorous genetic tests, the sodium channel change may be responsible for HyperPP in this patient and could also be responsible for the associated cardiac dysrhythmia.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Sodium channel protein type 4 subunit alphaP35499Details