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Hereditary cerebral hemorrhage with amyloidosis (HCHWA), Flemish type is a form of HCHWA characterized by an age of onset of 45 years of age, progressive Alzheimer's disease-like dementia and lobar intracerebral hemorrhage in some patients.
Biomarker and diagnostic research for ABetaA21G amyloidosis has been reported in the published literature.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for ABetaA21G amyloidosis.
110 publications have been identified in PubMed for ABetaA21G amyloidosis. Research spans Review / Meta-Analysis (72%), Case Report / Case Series (9%), and Other (8%).
Research Type | Count | % of Total |
|---|---|---|
Research summaries | 79 | 72% |
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 10:28 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about ABetaA21G amyloidosis
10 |
9% |
Other research | 9 | 8% |
Disease patterns and progression | 8 | 7% |
Laboratory research | 2 | 2% |
Testing and diagnosis research | 1 | 1% |
Clinical study results | 1 | 1% |
Cervantes CE (2026). [PMID: 38865984](https://pubmed.ncbi.nlm.nih.gov/38865984/). *Am J Nephrol*. [Review / Meta-Analysis]
Lavatelli F (2025). [PMID: 40669757](https://pubmed.ncbi.nlm.nih.gov/40669757/). *Matrix Biol*. [Review / Meta-Analysis]
Tang J (2025). [PMID: 41002209](https://pubmed.ncbi.nlm.nih.gov/41002209/). *R I Med J (2013)*. [Review / Meta-Analysis]
Donnelly JP (2025). [PMID: 41193074](https://pubmed.ncbi.nlm.nih.gov/41193074/). *J Hand Surg Am*. [Review / Meta-Analysis]
Self WK (2025). [PMID: 40590230](https://pubmed.ncbi.nlm.nih.gov/40590230/). *J Clin Invest*. [Other]
Cani L (2025). [PMID: 40090369](https://pubmed.ncbi.nlm.nih.gov/40090369/). *Br J Haematol*. [Review / Meta-Analysis]
Jamroziak K (2025). [PMID: 39748220](https://pubmed.ncbi.nlm.nih.gov/39748220/). *Br J Haematol*. [Review / Meta-Analysis]
Triposkiadis F (2025). [PMID: 39954876](https://pubmed.ncbi.nlm.nih.gov/39954876/). *Curr Probl Cardiol*. [Review / Meta-Analysis]
Ioannou A (2025). [PMID: 40650957](https://pubmed.ncbi.nlm.nih.gov/40650957/). *Future Cardiol*. [Review / Meta-Analysis]
Karam C (2025). [PMID: 41161999](https://pubmed.ncbi.nlm.nih.gov/41161999/). *Neurol Clin*. [Review / Meta-Analysis]
AI-curated news mentioning ABetaA21G amyloidosis
Updated Jul 8, 2026
A new treatment for children aged 2 or older with sickle cell disease has been approved by the U.S. Food & Drug Administration. In a press release on Wednesday, the FDA announced it had approved Casgevy, the first gene therapy for children with sickle cell disease. (NewsNation) — A new treatment for children aged 2 or older with sickle cell disease has been approved by the Food & Drug Administration (FDA). In a Wednesday news release, the FDA announced it had approved Casgevy, the first gene therapy for children with the disease. “Casgevy is a gene therapy consisting of the patient’s own (autologous) hematopoietic (blood) stem cells, administered as a one-time single dose for intravenous infusion,” the release noted. “Pediatric patients as young as 2 years of age can now access a critical additional treatment option to treat these debilitating, life-threatening diseases,” Karim Mikhail, the acting director of the Center for Biologics Evaluation and Research, wrote. “These disorders carry a heavy burden for children and their families, affecting growth, development, and long-term health in profound ways,” Megha Kaushal, acting deputy director of the Office of Therapeutic Products in CBER, said in the release.