This website provides information on patients with mutations in the ARL6 gene, including clinical data, molecular data, management, and research options.

Biallelic pathogenic variants in ARL6 gene are the genetic cause of Bardet-Biedl syndrome 3 (BBS3) and retinitis pigmentosa 55 (RP55).

This website was created to share and collect information about clinical, management, and research projects to gather more knowledge and provide better treatment of patients with mutations in the ARL6 gene.

Dr. Fowzan Alkuraya, MD (Hons) ABP ABMG, King Faisal Specialist Hospital and Research Center, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia, falkuraya@kfshrc.edu.sa

Fadie D. Altuame, MBBS, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia, faltuame@alfaisal.edu