Sander C
Kinderklinik, Stadtklinik Baden-Baden.
Monatsschr Kinderheilkd. 1988 Mar;136(3):149-50.
A case of familial hypokalemic periodic paralysis is discussed in a boy whose first paralysis occurred at 11 years of age. At first the paralysis was controlled by acetazolamid and potassium therapy. Later, frequent attacks of paralysis and muscle weakness developed necessitating a change of therapy. Diclofenamid has now already been administered for 2 years. It is well tolerated and has suppressed further attacks.
本文讨论了一名家族性低钾性周期性麻痹男孩的病例，该男孩首次发作麻痹是在11岁。起初，麻痹通过乙酰唑胺和钾疗法得到控制。后来，频繁发作的麻痹和肌无力出现，需要更换治疗方法。双氯非那胺现已使用2年。耐受性良好，且已抑制了进一步发作。
