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Biomarker and diagnostic research for hypoaldosteronism disease has been reported in the published literature.
1 clinical trial registered.
37 publications have been identified in PubMed for hypoaldosteronism disease. Research spans Case Report / Case Series (38%), Review / Meta-Analysis (24%), and Epidemiology / Natural History (14%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 14 | 38% |
Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 9:39 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
9 |
24% |
Disease patterns and progression | 5 | 14% |
Laboratory research | 4 | 11% |
Testing and diagnosis research | 3 | 8% |
Clinical study results | 1 | 3% |
New treatment approaches | 1 | 3% |
Free NW (2026). [PMID: 42117122](https://pubmed.ncbi.nlm.nih.gov/42117122/). *Oxf Med Case Reports*. [Case Report / Case Series]
Musa SA (2026). [PMID: 42255436](https://pubmed.ncbi.nlm.nih.gov/42255436/). *Front Endocrinol (Lausanne)*. [Case Report / Case Series]
da Cunha Brito P (2026). [PMID: 42223108](https://pubmed.ncbi.nlm.nih.gov/42223108/). *Endocr Connect*. [Review / Meta-Analysis]
Ahmed MMH (2026). [PMID: 41479431](https://pubmed.ncbi.nlm.nih.gov/41479431/). *Clin Case Rep*. [Case Report / Case Series]
Polycarpe C (2026). [PMID: 32310452](https://pubmed.ncbi.nlm.nih.gov/32310452/). *Unknown Journal*. [Review / Meta-Analysis]
Ruiz-Sánchez JG (2026). [PMID: 41802899](https://pubmed.ncbi.nlm.nih.gov/41802899/). *Endocrinol Diabetes Nutr (Engl Ed)*. [Epidemiology / Natural History]
Tariq HB (2026). [PMID: 41836828](https://pubmed.ncbi.nlm.nih.gov/41836828/). *Pak J Med Sci*. [Case Report / Case Series]
Yang J (2026). [PMID: 41889508](https://pubmed.ncbi.nlm.nih.gov/41889508/). *Front Med (Lausanne)*. [Gene Therapy / Novel Therapeutics]
Yang M (2026). [PMID: 41975049](https://pubmed.ncbi.nlm.nih.gov/41975049/). *Sci Rep*. [Epidemiology / Natural History]
Goi J (2026). [PMID: 41045519](https://pubmed.ncbi.nlm.nih.gov/41045519/). *J Clin Endocrinol Metab*. [Case Report / Case Series]
AI-curated news mentioning hypoaldosteronism disease
Updated Feb 6, 2026
Pfizer has initiated a Phase 3 trial for giroctocogene fitelparvovec (PF-07055480), a gene therapy targeting severe hemophilia A. This advancement reflects Pfizer's commitment to developing transformative treatments for rare diseases.
Rare Disease Day emphasizes the critical role of patient advocacy groups in driving research and treatment development for rare diseases. Celebrated annually on the last day of February, it aims to raise awareness and mobilize resources for conditions that often receive less attention.
Angela, Founder and President of Cal Rare, has significantly influenced rare disease advocacy in California, leading to the formation of the California Rare Disease Legislative Caucus, which now includes 25% of the State Legislature. Her recognition includes the Rare Voice Award for State Advocacy and accolades for her social media impact on rare disease awareness.
Amgen acquires Horizon Therapeutics for $27.3 billion, highlighting significant consolidation in the rare disease sector amid challenging financial conditions. This acquisition underscores the ongoing interest in rare disease therapies despite market difficulties.
Chiesi Farmaceutici acquired Amryt Pharma for up to $1.5 billion, while Ipsen purchased Albireo for up to $1.2 billion, marking a strong start for M&A in the rare disease sector in 2023. Despite these significant deals, overall financing in the sector remains weak.