Rare Neurometabolic Disorder: Investigating Leigh Syndrome with SURF1 Gene Mutations
Case Studies, RDRH
Born to non-consanguineous parents, perinatal asphyxia. Leigh Syndrome is a rare, inherited neurometabolic disorder that affects the central nervous system. It’s characterized by the progressive loss of mental and movement abilities.
Author
Dr. Nazmul Hamid
Pediatric Neurology & Development
Combined Military Hospital, Dhaka,
Bangladesh