Population
One family wherein individual members had clinical features of either paramyotonia congenita or hyperkalemic…
Design
Case_series
Authors
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May complicate distinguishing PC from HPP clinically; leaves open a unified genetic spectrum pending larger studies.
Paramyotonia congenita and hyperkalemic periodic paralysis may represent part of the spectrum of a single genetic disorder rather than distinct entities.
Silva et al. (1990) studied this question.
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