Bardet-Biedl Syndrome is a genetic condition, characterized by vision loss, excessive weight gain, extra fingers or toes, intellectual disability or problems learning, and abnormal genitalia.
Sites and pages in this category offer information about causes, diagnosis, management, prognosis, prevention, and genetics.
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European Journal of Human Genetics: Bardet-Biedl Syndrome
Includes characteristics, clinical overview, diagnostics, genetics, biology, management, and images.
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Foundation Fighting Blindness: Bardet-Biedl Syndrome
Furnishes definition, symptoms, treatment, and related diseases.
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GeneReviews: Bardet-Biedl Syndrome
Review of this condition by Waters, Aoife and Beales, Philip. Covers diagnosis, clinical description, management, and genetics.
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National Library of Medicine - BBS
Find the alternative names, a summary and the major features of Bardett-Biedl syndrome.
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NORD: Bardet Biedl Syndrome
Overview of the complex disorder, its symptoms, disorder subdivisions, and general discussion on the genetic inheritance of the said disease are provided.
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Patient.co.uk: Bardet-Biedl Syndrome
Physician-written, peer-reviewed article covers epidemiology, clinical features, diagnosis, management, prognosis, and prevention.