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Any ciliopathy caused by variants in the BBS4 gene.
Biomarker and diagnostic research for BBS4-related ciliopathy has been reported in the published literature.
No clinical trials have been registered for BBS4-related ciliopathy.
240 publications have been identified in PubMed for BBS4-related ciliopathy. Research spans Basic Science / Preclinical (39%), Review / Meta-Analysis (25%), and Epidemiology / Natural History (12%).
Research Type | Count | % of Total |
|---|---|---|
Laboratory research | 93 | 39% |
Data assembled from 2 of 12 sources · Last updated Sep 19, 2026, 6:46 AM UTC
Common questions about BBS4-related ciliopathy
61 |
25% |
Disease patterns and progression | 28 | 12% |
Patient case studies | 19 | 8% |
New treatment approaches | 19 | 8% |
Clinical study results | 10 | 4% |
Testing and diagnosis research | 8 | 3% |
Other research | 2 | 1% |
Gimpel C (2026). [PMID: 40965583](https://pubmed.ncbi.nlm.nih.gov/40965583/). *Pediatr Nephrol*. [Epidemiology / Natural History]
Akhila P (2026). [PMID: 41611321](https://pubmed.ncbi.nlm.nih.gov/41611321/). *BMJ Case Rep*. [Case Report / Case Series]
Guo DF (2026). [PMID: 41915029](https://pubmed.ncbi.nlm.nih.gov/41915029/). *Am J Physiol Cell Physiol*. [Basic Science / Preclinical]
Baker LW (2026). [PMID: 41130867](https://pubmed.ncbi.nlm.nih.gov/41130867/). *Eur J Intern Med*. [Review / Meta-Analysis]
Kuraoka S (2026). [PMID: 41742835](https://pubmed.ncbi.nlm.nih.gov/41742835/). *Adv Sci (Weinh)*. [Basic Science / Preclinical]
Duijzer R (2026). [PMID: 40793999](https://pubmed.ncbi.nlm.nih.gov/40793999/). *Liver Transpl*. [Epidemiology / Natural History]
Epting D (2026). [PMID: 40931526](https://pubmed.ncbi.nlm.nih.gov/40931526/). *HGG Adv*. [Case Report / Case Series]
Xiong Q (2026). [PMID: 41186985](https://pubmed.ncbi.nlm.nih.gov/41186985/). *J Am Soc Nephrol*. [Review / Meta-Analysis]
Brewer KM (2026). [PMID: 41512914](https://pubmed.ncbi.nlm.nih.gov/41512914/). *Developmental biology*. [Basic Science / Preclinical]
Hardy EP (2026). [PMID: 41748625](https://pubmed.ncbi.nlm.nih.gov/41748625/). *Nat Commun*. [Basic Science / Preclinical]
AI-curated news mentioning BBS4-related ciliopathy
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