Tsuchiya R, Nishimura R, Ito T
Arch Surg. 1977 Jan;112(1):82-4. doi: 10.1001/archsurg.1977.01370010084017.
We describe a 26-year-old man in whom the Laurence-Moon-Biedl-Bardet syndrome had been associated with congenital cystic dilations of both the intrahepatic and extrahepatic biliary tract. The fact of the simultaneous occurence of two rare diseases in a single patient suggests the congenital origin of cystic dilation of the biliary tract and the importance of examining for a possible association of anomalies in the alimentary tract with the Laurence-Moon-Biedl-Bardet syndrome.
我们描述了一名26岁男性，其劳伦斯-穆恩-比德尔-巴德特综合征与肝内和肝外胆道的先天性囊性扩张相关。单一患者同时出现两种罕见疾病这一事实提示胆道囊性扩张的先天性起源，以及检查消化道异常与劳伦斯-穆恩-比德尔-巴德特综合征可能关联的重要性。
