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.
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| http://dx.doi.org/10.1097/00005053-198104000-00011 | DOI Listing |
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