Bartter 氏综合征Bartter 氏综合征最初是对一5岁男孩作出这一诊断的,以后的报道大多亦系儿童。近来认为儿童病例是一种常染色体隐性遗传病。但本综合征的发病机理,迄未明瞭。切除两侧肾上腺,亦未能矫治患者病变,看来这是一种原发性肾性钾或氯化物流失。成人也有作出这一诊断的。但他们中间,很多都有导致慢性容量匮乏的特定病因,而使其病情可能类似 Bartter 氏综合征,故被称为假性 Bartt- Bartter’s Syndrome Bartter’s syndrome was originally diagnosed in a 5-year-old boy, most of whom were later reported as children. Recently considered a case of children is an autosomal recessive disease. However, the pathogenesis of this syndrome, as yet unknown. Excision of both adrenals, but also failed to correct the patient’s disease, it appears that this is a primary renal potassium or chloride loss. Adults also make this diagnosis. However, many of them have a specific etiology that leads to a chronic lack of capacity, making their condition similar to that of Bartter’s syndrome and therefore known as pseudo Bartt-