Ketogenic diet in children with epileptic encephalopathy

Kushairi, Sarah Syahirah (2025) Ketogenic diet in children with epileptic encephalopathy. Prescription (6): 15.

Abstract

Uncontrolled epileptic activity could lead to progression of cerebral dysfunction, resulting in a group of disorders called epileptic encephalopathy (EE). Lennox-Gastaut Syndrome (LGS) is a severe form of EE. It usually happens in children between 1-8 years old. Individuals with LGS could experience multiple types of seizures. LGS can be caused by a variety of conditions, including brain malformations and severe head injury. Most people with LGS experience some degree of impaired intellectual functioning/information processing, with developmental delays and behavioural disturbances.

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Item Type: Article
Creators:
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Kushairi, Sarah Syahirah
UNSPECIFIED
Subjects: R Medicine > RC Internal Medicine > Neuroscience. Biological psychiatry. Neuropsychiatry > Neurology. Diseases of the nervous system. Including speech disorders
R Medicine > RJ Pediatrics > Child Health. Child health services
Divisions: Universiti Teknologi MARA, Selangor > Puncak Alam Campus > Faculty of Pharmacy
Journal or Publication Title: Prescription
Number: 6
Keywords: Ketogenic diet, Epileptic encephalopathy
Date: June 2025
URI: https://ir.uitm.edu.my/id/eprint/120801
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