Original ResearchPublished 23 September 2026Utility of 3D facial analysis as a biomarker in rare diseases exploration with hereditary angioedemaSaumya Jamuar · Richard Palmer · Haur Yueh Lee · Faith Li-Ann Chia · Choo Beng Goh · Stuart Lee · Petra Helmholz · Shermaine Chan · Gareth BaynamFrontiers in Medical Technologydoi 10.3389/fmedt.2026.1857918
Original ResearchPublished 5 August 2026Diagnostic delay, SERPING1 allelic heterogeneity, and real-world lanadelumab prophylaxis in Chinese patients with hereditary angioedema due to C1 inhibitor deficiencyWenjin Du · Siqin Wang · Ke Yang · Qiuxing Zhang · Xianghua Lin · Wenchao Zhang · Weili GuoFrontiers in Allergydoi 10.3389/falgy.2026.1899305
Letter to the EditorPublished 7 July 2026Low C1q alone should not be taken as diagnostic of acquired angioedema in a kindred with familial type 1 C1-inhibitor deficiency and overlapping systemic lupus erythematosusAmane Takagi · Saori Takamura · Tomoo FukudaJournal of Cutaneous Immunology and Allergydoi 10.3389/jcia.2026.16999
