Systemic involvement in TREX1-associated familial chilblain lupus

Journal of the American Academy of Dermatology

Volumn 69, Issue 4, 2013, Pages

  Günther, Claudia ^a   Hillebrand, Matthias ^a   Brunk, Julia ^a   Lee Kirsch, Min Ae ^b  

^a DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

^b St Vinzenz und Elizabeth Hospital   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANTINUCLEAR ANTIBODY; HEMOGLOBIN; HYDROXYCHLOROQUINE; PREDNISOLONE;

ADULT; AICARDI GOUTIERES SYNDROME; ARTHRALGIA; AUTOIMMUNITY; CASE REPORT; CHILBLAIN; FAMILIAL CHILBLAIN LUPUS; GENE MUTATION; HEMOGLOBIN BLOOD LEVEL; HISTOLOGY; HUMAN; INTERPHALANGEAL JOINT; JOINT EFFUSION; JOINT SWELLING; KNEE PAIN; LABORATORY TEST; LETTER; LEUKOENCEPHALOPATHY; LEUKOPENIA; LIVER FUNCTION TEST; LUPUS VULGARIS; MALE; MEDICAL HISTORY; OTITIS; PANCYTOPENIA; PRIORITY JOURNAL; SEROLOGY; SHOULDER PAIN; SKIN LUPUS ERYTHEMATOSUS; SYNOVITIS; THROMBOCYTOPENIA; ULCER;

EID: 84884336624     PISSN: 01909622     EISSN: 10976787     Source Type: Journal    
DOI: 10.1016/j.jaad.2013.04.020     Document Type: Article

References (5)

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3. V. Tungler, R.M. Silver, H. Walkenhorst, C. Gunther, and M.A. Lee-Kirsch Inherited or de novo mutation affecting aspartate 18 of TREX1 results in either familial chilblain lupus or Aicardi-Goutières syndrome Br J Dermatol 167 2012 212 214
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