Mohammad Almuqbil

Pediatric Neurology & Neurogenetics Consultant, Associate Professor

Consultant in paediatric neurology and neurogenetics at King Abdullah Specialized Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard Health Affairs in Riyadh, and Associate Professor at King Saud bin Abdulaziz University for Health Sciences. He completed his paediatric neurology residency at McGill University in 2016, board training in medical genetics and genomics at Harvard Medical School in 2018, and a fellowship in medical biochemical genetics at Johns Hopkins University in 2019. His expertise covers paediatric neurological and neurogenetic disorders and rare diseases, and his published research spans neurogenetics, mitochondrial disorders and leukodystrophies, including a Saudi case series on parkinsonism-dystonia-2, work on the spectrum of FAR1 variants, and studies of aromatic L-amino acid decarboxylase deficiency in the Middle East. He serves on the boards of several scientific societies and takes part in training residents and fellows.