MeSH 搜索器

Werner Syndrome

An autosomal recessive disorder that causes premature aging in adults, characterized by sclerodermal skin changes, cataracts, subcutaneous calcification, muscular atrophy, a tendency to diabetes mellitus, aged appearance of the face, baldness, and a high incidence of neoplastic disease.
推出的年份: 1998
副标题
树号: C16.320.925, C18.452.284.960
MeSH 单一 ID: D014898
进入的组:
  • Syndrome, Werner
  • Adult Progeria
  • Werner's Syndrome
  • Syndrome, Werner's
  • Werners Syndrome
  • Syndrome, Werners
  • Adult Premature Aging Syndrome
  • Progeria, Adult

留言 (0)

沒有登入
gif