MeSH 搜索器

Leber Congenital Amaurosis

A rare degenerative inherited eye disease that appears at birth or in the first few months of life that results in a loss of vision. Not to be confused with LEBER HEREDITARY OPTIC NEUROPATHY, the disease is thought to be caused by abnormal development of PHOTORECEPTOR CELLS in the RETINA, or by the extremely premature degeneration of retinal cells.
推出的年份: 2010
副标题
树号: C11.270.516, C11.768.364
MeSH 单一 ID: D057130
进入的组:
  • Amauroses, Leber Congenital
  • Congenital Amauroses, Leber
  • Congenital Amaurosis, Leber
  • Leber Congenital Amauroses
  • Leber's Amaurosis
  • Amauroses, Leber's
  • Amaurosis, Leber's
  • Leber Amaurosis
  • Leber's Amauroses
  • Lebers Amaurosis
  • Leber Abiotrophy
  • Abiotrophies, Leber
  • Abiotrophy, Leber
  • Leber Abiotrophies
  • Leber Congenital Tapetoretinal Degeneration
  • Amaurosis, Leber Congenital
  • Congenital Retinal Blindness
  • Blindness, Congenital Retinal
  • Blindnesses, Congenital Retinal
  • Congenital Retinal Blindnesses
  • Retinal Blindnesses, Congenital
  • Congenital Amaurosis of Retinal Origin
  • Heredoretinopathia Congenitalis
  • Hereditary Retinal Aplasia
  • Dysgenesis Neuroepithelialis Retinae
  • Hereditary Epithelial Dysplasia of Retina
早前的内容:
  • Retinal Diseases (1963-2009)

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