本综合征是一种少见的先天畸形性疾病,并有遗传倾向。1866年由 Laurence 及Moon 二氏首先提出,1922年 Biedl 加以补充,至今全世界报告不足400例,国内仅见少数病例报告。现报告一例如下。刘×,男,12岁,1981年9月2日入院。患儿一个月来无任何诱因自觉心慌、气短、头晕,约持续几分钟后自行缓解,共发作6次。当地医院诊断为“心脏病?”,服药治疗无效而来院就医。父母非近亲结婚,父母及同胞姐弟均无类似疾 This syndrome is a rare congenital malformation disease, and genetic predisposition. First introduced by Laurence and Moon II in 1866 and supplemented by Biedl in 1922, less than 400 cases have been reported in the world to date, and only a few cases have been reported in the country. Here is an example of the report. Liu ×, male, 12 years old, admitted to hospital on September 2, 1981. Children with no incentive for a month to feel palpitated, shortness of breath, dizziness, about a few minutes to ease themselves after a total of 6 episodes. The local hospital diagnosed as “heart disease?”, Medication invalid and come to hospital for treatment. Parents are married to non-relatives, parents and siblings have no similar illness