: MeSH: Laurence-Moon Syndrome

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Abnormalities, Multiple > Laurence-Moon Syndrome

Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Hypothalamic Diseases > Laurence-Moon Syndrome

Laurence-Moon Syndrome

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An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY. This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity. (From N Engl J Med. 1989 Oct 12;321(15):1002-9)

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