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primary unilateral adrenal hyperplasia (PUAH) - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

primary unilateral adrenal hyperplasia

MONDO:0016504

Also known as:PUAH

Overview

Primary unilateral adrenal hyperplasia (PUAH) is a surgically-correctable form of primary (hyper) aldosteronism (PA) characterized by renin suppression, unilateral aldosterone hypersecretion, and moderate to severe hypertension secondary to hyperplasia of the adrenal gland.

Diagnosis

Biomarker and diagnostic research for primary unilateral adrenal hyperplasia has been reported in the published literature.

Prognosis

Estimated prevalence: Unknown (Unknown prevalence).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for primary unilateral adrenal hyperplasia.

49 publications have been identified in PubMed for primary unilateral adrenal hyperplasia. Research spans Case Report / Case Series (33%), Diagnostic / Biomarker (27%), and Review / Meta-Analysis (14%).

Research Type	Count	% of Total
Patient case studies	16	33%

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 1:07 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:231580

GARD

Genetic and Rare Diseases Info Center

GARD:20620

Questions for Your Care Team

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primary unilateral adrenal hyperplasia

Overview

Diagnosis

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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