TY - CHAP M1 - Book, Section TI - Familial Progressive Scleroderma A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Marciniak, Bruno A1 - Dalens, Bernard J. PY - 2006 T2 - Syndromes: Rapid Recognition and Perioperative Implications AB - Disorder characterized by progressive systemic sclerosis (scleroderma), calcium deposits (calcinosis) usually in the fingers, Raynaud syndrome, loss of muscle control of the esophagus (difficult swallowing), osseous deformity of the fingers (sclerodactyly), and small red spots (telangiectasia) on the skin (fingers, face) or inside the mouth. SN - PB - The McGraw-Hill Companies CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=58070648 ER -