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Results 1 - 3 of 3 for Familial chilblain lupus
  1. TREX1 gene 
    ... DE, Crow YJ. Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome. Am J Hum ...
    https://medlineplus.gov/genetics/gene/trex1 - Genetics
  2. Aicardi-Goutières syndrome 
    ... overlap with those of another disorder called systemic lupus erythematosus (SLE). A feature of SLE that also occurs in about 40 percent of people with Aicardi-Goutières syndrome is a skin problem called chilblains. Chilblains are painful, itchy skin lesions that are ...
    https://medlineplus.gov/.../condition/aicardi-goutieres-syndrome - Genetics
  3. Raynaud Phenomenon (National Library of Medicine)  
    ... to develop Raynaud phenomenon if you have a family member who has it. Secondary Raynaud phenomenon has been linked to: Certain diseases. These include lupus, scleroderma, rheumatoid arthritis (RA), carpal tunnel syndrome, and ...
    https://medlineplus.gov/raynaudphenomenon.html - Health Topics