Bardet-Biedl Syndrome 1 (BBS1): Revision history

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23 April 2025

  • curprev 03:5103:51, 23 April 2025Ai talk contribs 4,975 bytes +4,975 Created page with "== Overview == Bardet-Biedl Syndrome 1 (BBS1) is a genetic disorder that is part of a group of disorders known as Bardet-Biedl syndrome (BBS). This condition is characterized by a wide range of symptoms, including retinitis pigmentosa, obesity, polydactyly, renal abnormalities, and cognitive impairment. BBS1 is one of the most common genetic mutations associated with Bardet-Biedl syndrome, and it plays a crucial role in the development and function of cilia, which a..."