Bardet Biedel syndrome

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genetic disorder, hypogonadism, syndrome

Facts (generated by robot; please edit if you find it inaccurate)

• Bardet-Biedel syndrome is a spectacular example of this.
• Laurence-Moon-Bardet-Biedel syndrome is an autosomal recessive trait characterized by mental retardation, retinitis pigmentosa, polydactyly and hypogonadism.
• Bardet-Biedel syndrome is linked to DNA markers on chromosome 11q and is genetically heterogenous.
• Command Hospital (Southern Command), Pune-411040 Laurence-moon-bardet-biedel syndrome: presenting with acute onset of diabetes mellitus Medical Journal Armed Forces India.
• Phenotypes currently under study inclu 197 de retinoblastoma, retinitis pigmentosa, Leber congenital amaurosis, macular degeneration (see also age-related macular degeneration), Usher syndrome, and Bardet-Biedel syndrome.
• I have a very rare genetic syndrome called Lawrence Moon Bardet Biedel Syndrome (LMBBS) for short.

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