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Any Bardet-Biedl syndrome in which the cause of the disease is a mutation in the BBIP1 gene.
Features include always present findings: Stage 5 chronic kidney disease, Brachydactyly, Cataract, and Reduced kidney function (renal insufficiency) and others.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Kidneys and urinary system | 2 | Stage 5 chronic kidney disease, Reduced kidney function (renal insufficiency) |
BBIP1 encodes BBSome interacting protein 1 (92 aa). The BBSome complex is thought to function as a coat complex required for sorting of specific membrane proteins to the primary cilia. Highest expression in Testis (28.6 TPM) and Ovary (15.6 TPM).
Bardet-Biedl syndrome 18 is associated with mutations in the BBIP1 gene on chromosome 10.
The BBIP1 protein participates in HDAC6 deacetylates microtubules and ATAT acetylates microtubules pathways.
BBIP1 is classified as a druggable target with score 0.0.
Genetic testing for BBIP1 is available. Testing is considered confirmatory for diagnosis.
Biomarker and diagnostic research for Bardet-Biedl syndrome 18 has been reported in the published literature.
Phenotype severity distribution: 8 always present features.
No clinical trials have been registered for Bardet-Biedl syndrome 18.
21 publications have been identified in PubMed for Bardet-Biedl syndrome 18. Research spans Case Report / Case Series (37%), Clinical Trial Publication (16%), and Basic Science / Preclinical (16%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 7 | 37% |
Data assembled from 5 of 12 sources · Last updated Sep 19, 2026, 3:09 PM UTC
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
Common questions about Bardet-Biedl syndrome 18
Eyes
2 |
Cataract, Retinal dystrophy |
Brain and nerves | 1 | Intellectual disability |
Age of onset: middle age.
3 |
16% |
Laboratory research | 3 | 16% |
Disease patterns and progression | 3 | 16% |
Testing and diagnosis research | 2 | 11% |
Other research | 1 | 5% |
Argente J (2026). [PMID: 41703984](https://pubmed.ncbi.nlm.nih.gov/41703984/). *Obesity (Silver Spring)*. [Clinical Trial Publication]
Mahler EA (2026). [PMID: 41238926](https://pubmed.ncbi.nlm.nih.gov/41238926/). *Ophthalmologie*. [Other]
M R R (2026). [PMID: 41815617](https://pubmed.ncbi.nlm.nih.gov/41815617/). *Cureus*. [Case Report / Case Series]
Haqq AM (2025). [PMID: 39919037](https://pubmed.ncbi.nlm.nih.gov/39919037/). *J Clin Endocrinol Metab*. [Clinical Trial Publication]
Bouchoual M (2025). [PMID: 40852023](https://pubmed.ncbi.nlm.nih.gov/40852023/). *Ann Med Surg (Lond)*. [Case Report / Case Series]
Sridhar S (2025). [PMID: 40181855](https://pubmed.ncbi.nlm.nih.gov/40181855/). *Indian J Endocrinol Metab*. [Case Report / Case Series]
Pomeroy J (2025). [PMID: 40456618](https://pubmed.ncbi.nlm.nih.gov/40456618/). *Pediatr Obes*. [Epidemiology / Natural History]
Guo Z (2025). [PMID: 41331888](https://pubmed.ncbi.nlm.nih.gov/41331888/). *Zhonghua Wei Zhong Bing Ji Jiu Yi Xue*. [Epidemiology / Natural History]
Zmysłowska-Polakowska E (2025). [PMID: 41304128](https://pubmed.ncbi.nlm.nih.gov/41304128/). *Microorganisms*. [Basic Science / Preclinical]
Asghar A (2025). [PMID: 40384762](https://pubmed.ncbi.nlm.nih.gov/40384762/). *Mol Vis*. [Basic Science / Preclinical]
AI-curated news mentioning Bardet-Biedl syndrome 18
Updated Aug 25, 2026
The FDA approved Genglycos (pariglasgene brecaparvovec-opnr) to reduce daily cornstarch intake in patients aged 8 years and older with glycogen storage disease type Ia. Known as Von Gierke disease, GSDIa is a rare metabolic disorder caused by a mutation in the G6PC gene. This genetic variation leads to a deficiency in glucose-6-phosphatase (G6Pase), an enzyme needed to release glucose into the bloodstream. Without this enzyme, the body cannot properly maintain blood glucose levels, causing severe hypoglycemia and other serious metabolic complications · Pariglasgene brecaparvovec is an adeno-associated virus (AAV) serotype 8 based gene therapy that delivers a functional copy of the G6PC gene into liver cells, enabling the production of normally functioning G6Pase. Ultragenyx stated that as part of its postmarketing commitments to the FDA, the Company will provide 2 years of clinical data from open-label commercial treatment of 50 patients and 20 control patients through its existing GSDIa Disease Monitoring Program. ... Ultragenyx announces US FDA approval of Genglycos™ gene therapy, the first-ever FDA-approved treatment designed to treat the underlying cause of glycogen storage disease type Ia (GSDIa). “The reduced reliance on cornstarch, experienced by patients in our clinical studies, demonstrates this gene therapy’s ability to establish the normal breakdown of glycogen to produce glucose during fasting or episodes of metabolic stress. This ability to regulate glucose has alleviated the disease burden and has the potential to mitigate the risk of severe or life-threatening hypoglycemia for these patients.” Close more info about First Gene Therapy Approved for Glycogen Storage Disease Type la