Introduction: Huntington’s disease (HD) is considered a rare and fatal neurodegenerative disease; despite that, only one study described the outcomes among those with HD and COVID-19. In this context,
Patient ID, a specific number was assigned to each patient according to the chronology of their recruitment; Mutation, CFTR mutation for each patient was provided by the group of Pr. Taieb Messaoud at
Background: Primary hyperoxaluria type 1 (PH1) is a rare genetic disease that can result in irreversible damage to the kidneys and, eventually, extrarenal organs. While kidney failure is a known conse