MeSH 搜索器

Stargardt Disease

A juvenile-onset macular dystrophy characterized by progressive loss of VISUAL ACUITY with normal acuity in peripheral VISUAL FIELDS. Other associated clinical features may include LIPOFUSCIN fundus autofluorescence, atrophy of the RETINAL PIGMENT EPITHELIUM, loss of color vision, PHOTOPHOBIA and PARACENTRAL SCOTOMA. Germline mutations in the ABCA4 gene have been identified in recessive and dominant diseases.
推出的年份: 2020(2010)
副标题
树号: C11.270.872, C11.768.585.439.339, C16.320.290.724
MeSH 单一 ID: D000080362
进入的组:
  • Fundus Flavimaculatus
  • Stargardt Macular Degeneration
  • Degeneration, Stargardt Macular
  • Macular Degeneration, Stargardt
  • Stargardt Macular Degenerations
  • Stargardt Disease 1
  • Macular Dystrophy With Flecks, Type 1
  • Juvenile Macular Degeneration
  • Degeneration, Juvenile Macular
  • Juvenile Macular Degenerations
  • Macular Degeneration, Juvenile

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