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Hereditary disease by a qualitative or quantitative deficiencies or overexpression and/or abnormal accumulation of SERPIN; SERPINs are members of the serpin (serine proteinase inhibitors) superfamily which includes proteins with serine protease inhibitor activity and some that do not exhibit this inhibitory activity against serine proteases.
No clinical trials have been registered for serpinopathy.
3 publications have been identified in PubMed for serpinopathy. Research spans Review / Meta-Analysis (33%), Case Report / Case Series (33%), and Basic Science / Preclinical (33%).
Long LH (2026). [PMID: 42066914](https://pubmed.ncbi.nlm.nih.gov/42066914/). *J Allergy Clin Immunol*. [Basic Science / Preclinical]
Gariballa N (2024). [PMID: 38937821](https://pubmed.ncbi.nlm.nih.gov/38937821/). *J Biomed Sci*. [Review / Meta-Analysis]
Aggarwal S (2024). [PMID: 38831697](https://pubmed.ncbi.nlm.nih.gov/38831697/). *Clin Genet*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 12:47 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center