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Bardet-Biedl syndrome

Bardet-Biedl syndrome (BBS) is a genetic condition that affects multiple systems in the body. People with BBS may experience vision problems, obesity, kidney issues, and developmental delays. It is caused by mutations in several genes that are important for cell function. BBS is often recognized in childhood and can vary widely in symptoms and severity among individuals. It is a rare disorder, and management usually involves a team of healthcare providers to address the various challenges it presents, including vision care, weight management, and support for developmental needs.

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    Bardet-Biedl Syndrome (BBS) is a rare genetic disorder that affects multiple body systems. It is characterized by a combination of features, including obesity, vision loss due to retinal problems, kidney defects, extra fingers or toes, and learning difficulties. BBS results from mutations in certain genes that disrupt normal cell function. The symptoms can vary widely between individuals, making diagnosis challenging. While there is no cure, management focuses on treating specific symptoms and health issues to improve quality of life. Early diagnosis and a multidisciplinary approach can help address the various aspects of the syndrome.