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Any Bardet-Biedl syndrome in which the cause of the disease is a mutation in the SDCCAG8 gene.
Features include always present findings: Stage 5 chronic kidney disease, Short stature, Global developmental delay, and Reduced visual acuity and others; and common findings: Recurrent respiratory infections. 21 total HPO annotations.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Kidneys and urinary system | 5 | Renal dysplasia, Stage 5 chronic kidney disease, Reduced kidney function (renal insufficiency) |
SDCCAG8 function has not been fully characterized.
Bardet-Biedl syndrome 16 is caused by mutations in the SDCCAG8 gene on chromosome 1.
Genetic testing for SDCCAG8 is available. Testing is considered confirmatory for diagnosis.
Phenotype severity distribution: 7 always present features, 1 common feature.
No clinical trials have been registered for Bardet-Biedl syndrome 16.
19 publications have been identified in PubMed for Bardet-Biedl syndrome 16. Research spans Case Report / Case Series (47%), Epidemiology / Natural History (26%), and Basic Science / Preclinical (21%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 9 | 47% |
Data assembled from 6 of 12 sources · Last updated Sep 20, 2026, 3:06 PM UTC
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
Common questions about Bardet-Biedl syndrome 16
Lungs and breathing |
3 |
Respiratory distress, Bronchiolitis, Recurrent respiratory infections |
Brain and nerves | 3 | Global developmental delay, Difficulty with thinking and memory (cognitive impairment), Intellectual disability |
Ears | 2 | Hearing loss (hearing impairment), Recurrent otitis media |
Growth and development | 1 | Short stature |
Eyes | 1 | Retinal degeneration |
Blood and immune system | 1 | Recurrent respiratory infections |
Hormones | 1 | Hypogonadism |
Age of onset: adolescence.
5 |
26% |
Laboratory research | 4 | 21% |
New treatment approaches | 1 | 5% |
Milheiro J (2026). [PMID: 41940113](https://pubmed.ncbi.nlm.nih.gov/41940113/). *Clin Nephrol Case Stud*. [Case Report / Case Series]
Harvengt J (2025). [PMID: 40822950](https://pubmed.ncbi.nlm.nih.gov/40822950/). *Frontiers in endocrinology*. [Epidemiology / Natural History]
Haggerty K (2025). [PMID: 41333852](https://pubmed.ncbi.nlm.nih.gov/41333852/). *Obesity pillars*. [Case Report / Case Series]
Kuk M (2025). [PMID: 41048439](https://pubmed.ncbi.nlm.nih.gov/41048439/). *Frontiers in endocrinology*. [Case Report / Case Series]
Piekarska K (2025). [PMID: 41465080](https://pubmed.ncbi.nlm.nih.gov/41465080/). *Genes*. [Case Report / Case Series]
Fan X (2025). [PMID: 39856360](https://pubmed.ncbi.nlm.nih.gov/39856360/). *Scientific reports*. [Epidemiology / Natural History]
McEntee KE (2025). [PMID: 41279107](https://pubmed.ncbi.nlm.nih.gov/41279107/). *bioRxiv : the preprint server for biology*. [Basic Science / Preclinical]
Seyedtaghia MR (2025). [PMID: 40252141](https://pubmed.ncbi.nlm.nih.gov/40252141/). *Biochemical genetics*. [Basic Science / Preclinical]
Guo Z (2025). [PMID: 41331888](https://pubmed.ncbi.nlm.nih.gov/41331888/). *Zhonghua wei zhong bing ji jiu yi xue*. [Gene Therapy / Novel Therapeutics]
Li K (2025). [PMID: 40801568](https://pubmed.ncbi.nlm.nih.gov/40801568/). *Cells*. [Basic Science / Preclinical]
AI-curated news mentioning Bardet-Biedl syndrome 16
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