Hypokalemic Periodic Paralysis in a Young Woman With Mast Cell Activation Syndrome: A Case Report of an Atypical Presentation Associated With an Ultra‐Rare CACNA1S Variant

ABSTRACT Hypokalemic periodic paralysis (hKPP) is a rare neuromuscular channelopathy characterized by transient episodes of muscle weakness or paralysis associated with low serum potassium levels. It has been most commonly linked to autosomal dominant mutations in ion channel genes, specifically CAC...

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Autori principali:	Ali Moradi, Yasmin Aboutaleb, Saba Noreen, Abdullah Sahyouni, Hasin Sharma, Olugbenga Oyesanmi, Ian M. Kahane, Yizhi Lin, Hakan R. Toka
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Wiley 2026-06-01
Serie:	Clinical Case Reports
Soggetti:	CACNA1S mutation episodic paralysis hKPP hypokalemia hypokalemic periodic paralysis mast cell activation syndrome
Accesso online:	https://doi.org/10.1002/ccr3.72808
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