Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
Any ciliopathy caused by variants in the SDCCAG8 gene, including cases diagnosed as Bardet-Biedl syndrome 16 or Senior-Loken syndrome 7.
No clinical trials have been registered for SDCCAG8-related ciliopathy.
3 publications have been identified in PubMed for SDCCAG8-related ciliopathy. Research spans Basic Science / Preclinical (67%) and Gene Therapy / Novel Therapeutics (33%).
McEntee KE (2025). [PMID: 41279107](https://pubmed.ncbi.nlm.nih.gov/41279107/). *bioRxiv : the preprint server for biology*. [Gene Therapy / Novel Therapeutics]
Takahashi K (2025). [PMID: 39898911](https://pubmed.ncbi.nlm.nih.gov/39898911/). *Investigative ophthalmology & visual science*. [Basic Science / Preclinical]
Li K (2025). [PMID: 40801568](https://pubmed.ncbi.nlm.nih.gov/40801568/). *Cells*. [Basic Science / Preclinical]
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 9:40 PM UTC
Common questions about SDCCAG8-related ciliopathy