Liddle综合征(假性遗传性醛同酮增多症)是较罕见的疾病,现将本院收治1例报告如下,并对其诊断和治疗略加讨论。患者男性,15岁,主诉持续性高血压伴阵发性加剧4年,于1990年入院。1986年来患者常感头晕、头痛,血压波动在29～21/19～12kPa,频发剧烈头痛伴四肢冰冷,面色苍白,大汗淋漓。当地医院诊断 Liddle syndrome (pseudo-hereditary aldosteronism) is a rare disease, now admitted to our hospital a case report as follows, and its diagnosis and treatment of slightly discussed. Male patient, 15 years old, complained of persistent hypertension with paroxysmal aggravating 4 years, admitted to hospital in 1990. Patients often feel dizzy in 1986, headache, blood pressure fluctuations in 29 ~ 21/19 ~ 12kPa, frequent severe headache with extremities cold, pale, sweating. Local hospital diagnosis