Beitr Infusionther Klin Ernahr
February 1982
A case is reported of familial paroxysmal hypokalaemic paralysis, which postoperatively was complicated by a disturbance of carbohydrate metabolism. Paralysis commenced in a state of postoperative hypokalaemia and persisted afterwards in a state of severe hyperkalaemia. The intensive treatment is presented and the problem of episodic paralysis is widely discussed.
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