Telangiectasis in CREST syndrome and systemic sclerosis: correlation of clinical and pathological features with response to pulsed dye laser treatment

Author:

Halachmi Shlomit,Gabari Osama,Cohen Sarit,Koren Romelia,Amitai Dan Ben,Lapidoth Moshe

Publisher

Springer Science and Business Media LLC

Subject

Dermatology,Surgery

Reference19 articles.

1. Meyer O (1999) [From Thibierge–Weissenbach syndrome (1910) to anti-centromere antibodies (1980). Clinical and biological features of scleroderma]. Ann Med Interne (Paris) 150:47–52

2. Winterbauer RH (1964) Multiple telangiectasia, Raynaud’s phenomenon, sclerodactyly, and subcutanious calcinosis: a syndrome mimicking hereditary hemorrhagic telangiectasia. Bull Johns Hopkins Hosp 114:361–383

3. Frayha RA, Scarola JA, Shulman LE (1973) Calcinosis in scleroderma: a reevaluation of the CRST syndrome, abstracted. Arthritis Rheum 16:542

4. Velayos EE, Masi AT, Stevens MB, Shulman LE (1979) The 'CREST' syndrome. Comparison with systemic sclerosis (scleroderma). Arch Intern Med 139:1240–1244

5. Rouquette-Gally AM, Stern MH, Prost AC, Abuaf N, Homberg JC, Combrisson A (1985) Anti-centromere antibody, biological marker of the CREST syndrome as distinct from scleroderma. Presse Med 14:1497–1500

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