• 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.
(Arch Surg 112:82-84, 1977)
Tsuchiya R, Nishimura R, Ito T. Congenital Cystic Dilation of the Bile Duct Associated With Laurence-Moon-Biedl-Bardet Syndrome. Arch Surg. 1977;112(1):82-84. doi:10.1001/archsurg.1977.01370010084017