Clinical spectrum and geographic distribution of keratitis fugax hereditaria caused by the pathogenic variant c.61G>C in NLRP3

Purpose To chart clinical findings in individuals with keratitis fugax hereditaria (KFH) and the geographic distribution of their ancestors. Methods Patient population included 84 Finnish patients (55% female) from 25 families with the pathogenic NLRP3 variant c.61G>C. Procedures and main outcome...

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Veröffentlicht in:Acta ophthalmologica (Oxford, England) England), 2022-01, Vol.100 (S267), p.n/a
Hauptverfasser: Immonen, Annamari, Kawan, Sabita, Vesaluoma, Minna, Heiskanen, Miikael, Taipale, Claudia, Koskinen, Mira, Majander, Anna, Kivelä, Tero, Turunen, Joni
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