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Laurence-Moon-Biedl syndrome and Laurence-Moon-Biedl-Bardet redirect here. See below for an explanation.

The Bardet-Biedl syndrome is a genetic disorder characterized mainly by obesity, pigmentary retinopathy, polydactyly, mental retardation, hypogonadism, and renal failure in fatal cases.

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Genetic Disorders
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genetics & clinical characteristics of bardet-biedl syndrome http://bit.ly/752qwk
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National Library of Medicine - A summary of Bardet-Biedl syndrome and a list of major features.

NORD: Bardet Biedl Syndrome - Offers a general discussion along with further resources.
Meta Description: [ National Organization for Rare Disorders is dedicated to helping people with rare, orphan diseases. Rarediseases.org contains information on the prevention, treatment and cure of rare diseases. ]

Readers Digest Health - Bardet-Biedl syndrome: General information and resources.
Meta Description: [ Treat your body right. We've got a wealth of information about everything from allergies to weight loss to keep yourself and your loved ones well. ]

The CaF Directory - Information about Laurence-moon-bardet-biedl syndrome, its symptoms and inheritance patterns.
Meta Description: [ Contact a Family is a UK charity for families with disabled children. We offer information on specific conditions and rare disorders. ]

500 UMDS: LMBBS - Information for health-care professionals involved in the care of Laurence-Moon-Bardet-Biedl Syndrome patients and for parents or relatives seeking education on the syndrome.

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