MeSH 搜索器

Pseudoxanthoma Elasticum

An inherited disorder of connective tissue with extensive degeneration and calcification of ELASTIC TISSUE primarily in the skin, eye, and vasculature. At least two forms exist, autosomal recessive and autosomal dominant. This disorder is caused by mutations of one of the ATP-BINDING CASSETTE TRANSPORTERS. Patients are predisposed to MYOCARDIAL INFARCTION and GASTROINTESTINAL HEMORRHAGE.
推出的年份:
副标题
树号: C14.907.454.530, C15.378.463.515.530, C16.131.831.766, C16.320.850.750, C17.300.766, C17.800.804.766, C17.800.827.750
MeSH 单一 ID: D011561
进入的组:
  • Gronblad-Strandberg Syndrome
  • Gronblad Strandberg Syndrome
  • Syndrome, Gronblad-Strandberg
  • Groenblad-Strandberg Syndrome
  • Pseudoxanthoma Elasticum, Incomplete
  • Elasticum, Incomplete Pseudoxanthoma
  • Elasticums, Incomplete Pseudoxanthoma
  • Incomplete Pseudoxanthoma Elasticum
  • Incomplete Pseudoxanthoma Elasticums
  • Pseudoxanthoma Elasticums, Incomplete
  • Pseudoxanthoma Elasticum, Autosomal Dominant
  • Pseudoxanthoma Elasticum, Forme Fruste

留言 (0)

沒有登入
gif