Leber Congenital Amaurosis (LCA): Potential for Improvement of Vision

Eitemau Tebyg

• Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: Retained photoreceptors adjacent to retinal disorganization
  gan: Jacobson, Samuel G., et al.
  Cyhoeddwyd: (2009)
• Defining the Residual Vision in Leber Congenital Amaurosis Caused by RPE65 Mutations
  gan: Jacobson, Samuel G., et al.
  Cyhoeddwyd: (2008)
• Treatment Potential for LCA5-Associated Leber Congenital Amaurosis
  gan: Uyhazi, Katherine E., et al.
  Cyhoeddwyd: (2020)
• Vision 1 Year after Gene Therapy for Leber’s Congenital Amaurosis
  gan: Cideciyan, Artur V., et al.
  Cyhoeddwyd: (2009)
• Treatment Potential for Macular Cone Vision in Leber Congenital Amaurosis Due to CEP290 or NPHP5 Mutations: Predictions From Artificial Intelligence
  gan: Sumaroka, Alexander, et al.
  Cyhoeddwyd: (2019)