definition
This form of systemic scleroderma is usually less severe than other forms, consisting of calcinosis cutis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, and telangiectasis. If there is no esophageal dysfunction present, the disorder is is known as CRST syndrome. These forms of scleroderma are rare in children.
UMLS
Calc/Rayn/sclerodact/oes/telan, Calcinos, Raynaud, sclerodactyly, esophageal, telangiect, Calcinos, Raynaud, sclerodactyly, oesophageal, telangiect, Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly and telangiectasia, Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal dysfunction, telangiectasia syndrome, Calcinosis, Raynaud's phenomenon, sclerodactyly, oesophageal dysfunction, telangiectasia syndrome, CREST, CREST - Calc, Raynaud, sclerodact, oesoph, telangiect, CREST - Calc,Rayn phen,oesoph dysf,sclerodact,telangiectasia, CREST - Calc/Rayn/scl/oes/tel, CREST - Calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia, CREST - Calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly, telangiectasia, CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal involvement, telangiectasia synd, CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, oesophageal involvement, telangiectasia syn, CREST Syndrome, CREST VARIANT OF SCLERODERMA, Syndrome, CREST