Keratoendotheliitis Fugax Hereditaria A Novel CryopyrinAssociated Periodic Syndrome

Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP 3) Gene Joni A. Turunen, Juho Wedenoja, Pauliina Repo, Reetta-Stiina Järvinen, Johannes E. Jäntti, Sanna Mörtenhumer, Antti S. Riikonen, Anna-Elina Lehesjoki, Anna Majander, Tero T. Kivelä American Journal of Ophthalmology Volume 188 Pages 41 -50 (April 2018) DOI: 10. 1016/j. ajo. 2018. 017 Copyright © 2018 The Author(s) Terms and Conditions

Figure 1 American Journal of Ophthalmology 2018 18841 -50 DOI: (10. 1016/j. ajo. 2018. 017) Copyright © 2018 The Author(s) Terms and Conditions

Figure 2 American Journal of Ophthalmology 2018 18841 -50 DOI: (10. 1016/j. ajo. 2018. 017) Copyright © 2018 The Author(s) Terms and Conditions

Figure 3 American Journal of Ophthalmology 2018 18841 -50 DOI: (10. 1016/j. ajo. 2018. 017) Copyright © 2018 The Author(s) Terms and Conditions

Figure 4 American Journal of Ophthalmology 2018 18841 -50 DOI: (10. 1016/j. ajo. 2018. 017) Copyright © 2018 The Author(s) Terms and Conditions

Figure 5 American Journal of Ophthalmology 2018 18841 -50 DOI: (10. 1016/j. ajo. 2018. 017) Copyright © 2018 The Author(s) Terms and Conditions

American Journal of Ophthalmology 2018 18841 -50 DOI: (10. 1016/j. ajo. 2018. 017) Copyright © 2018 The Author(s) Terms and Conditions