Rare Neurometabolic Disorder: Investigating Leigh Syndrome with SURF1 Gene Mutations

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
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