1985年5月在我科确诊特发性甲状腺机能减退(简称IHP)合并两侧大脑基底结钙化1例。此疾病我区尚未见报告,现报道1例,并略作讨论。患者,女,34岁,因发作性两手足搐搦一个月,于1985年5月4日来我院就诊。患者来我院前的一个月曾在某医院留医,发病情况是突然有手足搐搦,手呈鹰爪状,同时有四肢疼痛,发作时神志清楚;发作前有喉部紧感、气逼等先兆,数分钟后即搐搦;一个月内共发作九次,每次持续约10～30分钟,用钙剂静注能使发作缓解至停止。该院诊断为植物神经功能紊乱。患者半年来感四肢易麻木,过去无搐搦史,无甲状腺手术史及放疗史,一向康健, 1985 May in our department diagnosed idiopathic hypothyroidism (IHP) combined with bilateral calcification of the basal ganglia in 1 case. The disease has not yet been reported in our area, is reported in 1 case, and a little discussion. The patient, female, 34 years old, came to our hospital on May 4, 1985 for one month because of episodic bipolar disorder. The patient came to a hospital a month before my hospital, the incidence of sudden tetany, the hand was eagle-shaped, with limb pain, the onset of consciousness; pre-seizure tightness of the throat, forced aura such as , Convulsions after a few minutes; a total of nine times within a month, each lasting about 10 to 30 minutes, with intravenous calcium can make the attack eased to a halt. The hospital diagnosed as autonomic dysfunction. Six months in patients with limb numbness, past no convulsions history, no history of thyroid surgery and radiotherapy history, has always been healthy,