Exploring the neurophysiologic and neuropathologic basis of visual deficits in cystinosis
Hayley Chang, Landa Prifti, Alexander Solorzano, Cristina Canavesi, Ed Freedman, Kuan Wang, John Foxe · FENS Forum 2024
Cystinosis is a rare, childhood lysosomal storage disorder caused by mutations in cystinosin, the transporter responsible for cystine from the lysosome to the cytosol. In cystinosis, mutated cystinosin causes cystine crystal accumulation and cell death. Photophobia, or abnormal sensitivity to light, is an early symptom of the disease and can be debilitating for patients. Historically, this photophobia has been attributed to ocular corneal cystine crystal accumulation, but eyedrops prescribed to disrupt these crystals do not fully alleviate symptoms. Furthermore, photophobia is known to have a
ePoster · Neuroscience