Gazdíková K, Gazdík F
Klinika farmakoterapie Ustavu preventívnej a klinickej medicíny, Bratislava.
Cas Lek Cesk. 2003 Aug;142(8):474-8.
Hypokalemia is associated with some renal diseases manifested by renal tubular acidosis (type I and II) or by renal tubular syndrome (Bartter's, Gitelman's and Liddle's syndrome). Bartter's syndrome, originally described by Batter and colleagues in 1962, is a set of closely related renal tubular disorders characterized by hypokalemia, hypochloremia, metabolic alkalosis and hyperreninemia with normal blood pressure. The underlying renal abnormality results in excessive urinary losses of sodium, chloride, potassium and calcium. Muscle weakness, polydipsia, polyuria and mental retardation can be also present. Affected children have poor growth rates and they appear malnourished. The article is focused on ethiopathogenesis, laboratory and clinical characteristics and on the treatment of Bartter's syndrome.
低钾血症与一些以肾小管酸中毒(I型和II型)或肾小管综合征(巴特综合征、吉特曼综合征和利德尔综合征)为表现的肾脏疾病相关。巴特综合征最初由巴特及其同事在1962年描述,是一组密切相关的肾小管疾病,其特征为低钾血症、低氯血症、代谢性碱中毒和高肾素血症,血压正常。潜在的肾脏异常导致钠、氯、钾和钙的尿排泄过多。还可能出现肌肉无力、多饮、多尿和智力发育迟缓。患病儿童生长速度缓慢,看起来营养不良。本文重点关注巴特综合征的发病机制、实验室和临床特征以及治疗方法。