Mesh term CREST Syndrome
Browse to parent terms:Calcinosis
Esophageal Motility Disorders
Raynaud Disease
Scleroderma, Limited
Telangiectasis
Description
A mild form of LIMITED SCLERODERMA, a multi-system disorder. Its features include symptoms of CALCINOSIS; RAYNAUD DISEASE; ESOPHAGEAL MOTILITY DISORDERS; sclerodactyly, and TELANGIECTASIS. When the defect in esophageal function is not prominent, it is known as CRST syndrome.Search for this term in our Faculty Database
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