An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene

• Asıl Yazarlar: Yang Hee Park (Yazar), June Bum Kim (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Korean Pediatric Society, 2010-10-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

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...