Case Report: Diagnostic difficulties, treatment, and association of the MEFV E148Q variant in a patient with PASH syndrome
This case report represents the first documentation of a PASH syndrome patient carrying the homozygous E148Q variant. Adalimumab demonstrated good therapeutic efficacy; however, disease recurrence occurred due to poor medication adherence, highlighting the importance of long-term management. The pathogenicity of E148Q alone is relatively weak and likely depends on polygenic accumulation or epigenetic dysregulation. It may contribute to disease pathogenesis through a "variant load" mechanism in conjunction with ethnic differences and other genetic or environmental factors.
Authors
- Jiarong Liang (ORCID: https://orcid.org/0000-0002-1990-6780)
- Cunwei Cao (ORCID: https://orcid.org/0000-0002-6279-0322)
- Qiang Qin
- Bingkun Li (ORCID: https://orcid.org/0000-0003-1755-9620)
- Jiaguang Su
Institutions
- Tung Fang Design Institute (TW)
- Guangxi Medical University (CN)
- First Affiliated Hospital of GuangXi Medical University (CN)
- Guangxi Center for Disease Prevention and Control (CN)
Publication Details
- Journal
- Frontiers in Medicine
- Published
- 2025-08-08
- DOI
- https://doi.org/10.3389/fmed.2025.1557540
- Citations
- 1
- Primary Topic
- Inflammasome and immune disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.81
Funders
- National Key Research and Development Program of China