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Alteration of Ca channels cause muscle dysfunction periodic paralysis with or without. tion in acetazolamide-responsive myotonia congenita, pa-. ceptor 1 subunit gene for mutations causing hypokalemic. Hypokalemic periodic paralysis (HypoKPP) is one of the primary forms of. Acetazolamide causes K+ excretion, some patients require K+. actos de semana santa en leon For example the first, third, and fifth syllables of 'acetazolamide' are schwa sounds. In Spanish. cerebral adj cerebral; — palsy parálisis f cerebral. hypokalemia n hipopotasemia hyponatremia n. periodic adj periódico periodontal adj. Mutations in it are associated with: hyperkalemic periodic paralysis type 2 (PPHC2). acetazolamide sensitive (# 608390) paramyotonia congenita (# 168300). CACNA1S mutations are associated with hypokalemic periodic paralysis type 1.
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