Bardet-Biedl syndrome 15

Bardet-Biedl syndrome 15 is a rare condition that is part of the Bardet-Biedl syndrome group. This condition is specifically caused by a mutation in the WDPCP gene. People with Bardet-Biedl syndrome may experience a range of symptoms, although the exact details can vary. The genetic change disrupts normal development and function in various parts of the body. Bardet-Biedl syndrome 15 is defined by its underlying genetic cause. The condition is identified by testing for changes in the WDPCP gene. Information provided from trusted sources such as OMIM and GARD supports a clear genetic basis for this disorder. This summary intends to provide a simple overview based on current available definitions.

Information about symptoms is currently limited for this condition.

Bardet-Biedl syndrome 15 is caused by a mutation in the WDPCP gene. This change in the gene affects normal body development and function, and it is a known factor in this specific type of Bardet-Biedl syndrome.

Information about treatment is currently limited for this condition.

Information about prognosis is currently limited for this condition.

Information about research is currently limited for this condition.