An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene
Familial hypokalemic periodic paralysis is an autosomal-dominant channelopathy characterized by episodic muscle weakness with hypokalemia. The respiratory and cardiac muscles typically remain unaffected, but we report an atypical case of a family with hypokalemic periodic paralysis in which the affe...
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| Main Authors: | , |
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| Format: | Book |
| Published: |
Korean Pediatric Society,
2010-10-01T00:00:00Z.
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