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Letter to the Editor

A hereditary clue for the development of cutaneous polyarteritis nodosa in siblings

Page 721 | Received 07 Sep 2016, Accepted 19 Sep 2016, Published online: 27 Oct 2016

References

  • Kizawa T, Yoto Y, Mizukami M, Tsugawa T, Takeuchi T, Kamasaki H, et al. A case report of cutaneous polyarteritis nodosa in siblings. Mod Rheumatol. 2016;. doi: 10.1080/14397595.2016.1189139.
  • Migita K, Izumi Y, Jiuchi Y, Iwanaga N, Kawahara C, Agematsu K, et al. Familial Mediterranean fever is no longer a rare disease in Japan. Arthritis Res Ther. 2016;. doi: 10.1186/s13075-016-1071-5.
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  • Eleftheriou D, Dillon MJ, Tullus K, Marks SD, Pilkington C. a, Roebuck DJ, et al. Systemic polyarteritis nodosa in the young: a single-center experience over thirty-two years. Arthritis Rheum. 2013;65:2476–85.
  • Mason JC, Cowie MR, Davies KA, Schofield JB, Cambridge J, Jackson J, et al. Familial polyarteritis nodosa. Arthritis Rheum. 1994;37:1249–53.

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