Weiss M, Meshulam B, Wijsenbeek H
J Nerv Ment Dis. 1981 Apr;169(4):259-60. doi: 10.1097/00005053-198104000-00011.
The Laurence-Moon-Biedl-Bardet syndrome is probably transmitted hereditarily and recognizable mainly by: a) retinitis pigmentosa; b) hypogonadism and obesity; and c) orthopedic anomalities such as polidactylia, syndactylia, and acroecephalosyndactylia with oligophrenia. Sometimes, other disturbance, mainly dermatological (alopecia), neurological, urological, endocrinological, and, rarely, congenital heart defects, may coexist.
劳伦斯-穆恩-比德尔-巴德特综合征可能通过遗传传递，主要通过以下方面识别：a) 色素性视网膜炎；b) 性腺功能减退和肥胖；c) 骨科异常，如多指畸形、并指畸形以及尖头并指畸形伴智力发育迟缓。有时，可能并存其他病症，主要是皮肤病学方面的（脱发）、神经学、泌尿学、内分泌学方面的，以及极少出现的先天性心脏缺陷。
