Dravet syndrome (DS) is a rare severe epilepsy syndrome associated with slowed
psychomotor development and behavioral disorders from the second year onward in a …

Gait abnormality detection is critical for the early discovery and progressive tracking of
musculoskeletal and neurological disorders, such as Parkinson's and Cerebral Palsy …

Abnormalities of human walking are critical indicators for the early detection of the risk of
trips and falls and of neuromusculoskeletal disorders such as joint impairments, Parkinson's …

Dravet syndrome (DS) is a rare and severe form of genetic epilepsy characterized by
cognitive and behavioural impairments and progressive gait deterioration. The …

Dravet syndrome (DS) is a rare and severe form of epilepsy that typically manifests in
children, which occur due to loss-of-function mutations in SCN1A gene. Despite advances in …

Dravet syndrome is a rare developmental epileptic encephalopathy starting in infancy 1. A
mutation in the voltage-gated sodium channel alpha subunit 1 (SCN1A) gene is reported in …