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Any inflammatory bowel disease in which the cause of the disease is a mutation in the ALPI gene.
Biomarker and diagnostic research for ALPI-related inflammatory bowel disease has been reported in the published literature.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for ALPI-related inflammatory bowel disease.
205 publications have been identified in PubMed for ALPI-related inflammatory bowel disease. Kisho has analyzed 148 by research type. Research spans Review / Meta-Analysis (78%), Other (9%), and Basic Science / Preclinical (7%).
Research Type | Count | % of Total |
|---|---|---|
Research summaries | 115 | 78% |
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 2:21 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about ALPI-related inflammatory bowel disease
Other research
13 |
9% |
Laboratory research | 11 | 7% |
Testing and diagnosis research | 4 | 3% |
Clinical study results | 2 | 1% |
Disease patterns and progression | 2 | 1% |
New treatment approaches | 1 | 1% |
Liang L (2026). [PMID: 41614418](https://pubmed.ncbi.nlm.nih.gov/41614418/). *Int J Mol Med*. [Review / Meta-Analysis]
Massironi S (2026). [PMID: 41445380](https://pubmed.ncbi.nlm.nih.gov/41445380/). *Inflamm Bowel Dis*. [Other]
Chen H (2026). [PMID: 41722201](https://pubmed.ncbi.nlm.nih.gov/41722201/). *Transl Oncol*. [Epidemiology / Natural History]
Choi J (2026). [PMID: 42055298](https://pubmed.ncbi.nlm.nih.gov/42055298/). *J Control Release*. [Review / Meta-Analysis]
Lee J (2026). [PMID: 41519836](https://pubmed.ncbi.nlm.nih.gov/41519836/). *Sci Rep*. [Basic Science / Preclinical]
Williams S (2026). [PMID: 41711045](https://pubmed.ncbi.nlm.nih.gov/41711045/). *J Crohns Colitis*. [Review / Meta-Analysis]
Castillo FA (2026). [PMID: 40845931](https://pubmed.ncbi.nlm.nih.gov/40845931/). *Immunol Lett*. [Review / Meta-Analysis]
Xie J (2026). [PMID: 42123495](https://pubmed.ncbi.nlm.nih.gov/42123495/). *Int J Mol Sci*. [Review / Meta-Analysis]
Devi J (2026). [PMID: 41581945](https://pubmed.ncbi.nlm.nih.gov/41581945/). *Gastroenterol Clin North Am*. [Review / Meta-Analysis]
Zheng S (2026). [PMID: 42136636](https://pubmed.ncbi.nlm.nih.gov/42136636/). *Front Immunol*. [Review / Meta-Analysis]
AI-curated news mentioning ALPI-related inflammatory bowel disease
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