American journal of ophthalmology۲۰۲۵نمایه شده در PubMed
Annamari T Immonen, Sabita Kawan, Michael P Backlund, Heikki Saaren-Seppälä, Tero T Kivelä, Joni A Turunen
چکیده
To study errors and delays in diagnosing keratitis fugax hereditaria (KFH), an autosomal-dominant periodic corneal autoinflammatory disease caused by the NLRP3 variant c.61G>C, by reviewing the medical records of genetically confirmed Finnish patients with KFH and by determining the frequency of…
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DOI: 10.1016/j.ajo.2025.03.004