Acta ophthalmologica۲۰۲۶نمایه شده در PubMed
Annamari T Immonen, Sara P Luostarinen, Päivi Lahermo, Sabita Kawan, Kati Donner, Joseph D Terwilliger, Michael P Backlund, Joni A Turunen
چکیده
To investigate the genetic and genealogical background of keratitis fugax hereditaria (KFH), a periodic corneal disease caused by the heterozygous pathogenic variant c.61G>C in the NLRP3 gene. KFH is characterized by recurrent unilateral autoinflammatory attacks alternating between the eyes and…
متن کامل چکیده در سایت ناشر در دسترس است.
DOI: 10.1111/aos.70238