中国神经再生研究(英文版) ›› 2022, Vol. 17 ›› Issue (8): 1755-1756.doi: 10.4103/1673-5374.332148

• 观点:神经损伤修复保护与再生 • 上一篇    下一篇

基因疗法治疗神经元类脂质炎

  

  • 出版日期:2022-08-15 发布日期:2022-01-22

Ocular therapies for neuronal ceroid lipofuscinoses: more than meets the eye

Samantha J. Murray, Nadia L. Mitchell*   

  1. Faculty of Agricultural and Life Sciences, Lincoln University, Lincoln, New Zealand
  • Online:2022-08-15 Published:2022-01-22
  • Contact: Nadia L. Mitchell, PhD, Nadia.Mitchell@lincoln.ac.nz.

摘要: https://orcid.org/0000-0003-4801-2804 (Nadia L. Mitchell)

Abstract: The neuronal ceroid lipofuscinoses (NCLs), also known as Batten disease, are a group of inherited, neurodegenerative, lysosomal storage diseases typically manifesting in childhood. There are currently 13 known forms of NCL resulting from various mutations in the CLN (ceroid lipofuscinoses neuronal) genes (CLN1-8 and CLN10-14). Although varying in onset and severity, the NCLs share several phenotypic features including seizures, motor dysfunction, cognitive decline, and progressive loss of vision (Mole et al., 2011). Current treatment strategies being investigated in pre-clinical studies and early stage clinical trials primarily target the brain and spinal cord. While these potential therapeutics show promise in attenuating neurological disease, protection against retinal dysfunction and degeneration is generally ineffective or not reported.