search

MeSH 搜索器

CREST Syndrome

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.
推出的年份: 1994
副标题
树号: C06.405.117.119.500.204, C14.907.617.812.500, C14.907.823.225, C17.300.799.801.500, C17.800.784.801.500, C18.452.174.130.204
MeSH 单一 ID: D017675
进入的组:
  • CREST Syndromes
  • Syndrome, CREST
  • Calcinosis, Raynaud's phenomenon, Esophageal dismobility, Sclerodactyly, Telangiectasia Syndrome
  • CRST Syndrome
  • CRST Syndromes
  • Syndrome, CRST
  • Calcinosis-Raynaud Phenomenon-Sclerodactyly-Telangiectasia
  • Calcinosis Raynaud Phenomenon Sclerodactyly Telangiectasia
  • Phenomenon-Sclerodactyly-Telangiectasia, Calcinosis-Raynaud
早前的内容:
  • Calcinosis (1975-1993)
  • Raynaud's Disease (1975-1993)
  • Scleroderma, Systemic (1975-1993)

留言 (0)

沒有登入
gif