MeSH 搜索器

Familial Exudative Vitreoretinopathies

A group of inherited disorders characterized by incomplete development of the retinal vasculature. Its severity can vary from complete blindness in infancy, to mild or no visual problems, where small areas of vascular defects are observable only by FLUORESCEIN ANGIOGRAPHY. Exudative vitreoretinopathy 1 is associated with mutations in the FZD4 gene.
推出的年份: 2020(2014)
副标题
树号: C11.250.345, C11.270.238, C11.768.337, C16.131.384.424, C16.320.290.352
MeSH 单一 ID: D000080345
进入的组:
  • Exudative Vitreoretinopathy, Familial
  • Vitreoretinopathy, Familial Exudative
  • Familial Exudative Vitreoretinopathy
  • X-Linked Familial Exudative Vitreoretinopathy
  • X Linked Familial Exudative Vitreoretinopathy
  • XL-FEVR

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