Chilblains in Southern California: two case reports and a review of the literature
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine
Link
http://link.springer.com/content/pdf/10.1186/1752-1947-8-381.pdf
Reference15 articles.
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2. Sugiura K, Takeichi T, Kono M, Ito Y, Ogawa Y, Muro Y, Akiyama M: Severe chilblain lupus is associated with heterozygous missense mutations of catalytic amino acids or their adjacent mutations in the exonuclease domains of 3'-repair exonuclease 1. J Invest Dermatol. 2012, 132: 2855-2857. 10.1038/jid.2012.210.
3. Abe J, Izawa K, Nishikomori R, Awaya T, Kawai T, Yasumi T, Hiragi N, Hiragi T, Ohshima Y, Heike T: Heterozygous TREX1 p.Asp18Asn mutation can cause variable neurological symptoms in a family with Aicardi–Goutières syndrome/familial chilblain lupus. Rheumatology. 2012, 52: 406-408.
4. Gunther C, Meurer M, Stein A, Viehweg A, Lee-Kirsch MA: Familial chilblain lupus – A monogenic form of cutaneous lupus erythematosus due to a heterozygous mutation in TREX1. Dermatology. 2009, 219: 162-166. 10.1159/000222430.
5. Prakash S, Weisman MH: Idiopathic chilblains. Am J Med. 2009, 122: 1152-1155. 10.1016/j.amjmed.2009.07.011.
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