We read with interest the Article reporting findings of the KIWE trial,1 which compared the ketogenic diet with antiseizure medications in infants with drug-resistant epilepsy.

Infantile Hypotonia with Psychomotor Retardation and Characteristic Facies-3 (IHPRF-3) Syndrome is a rare pathology occurring due to mutations in the TBC1 domain containing kinase (TBCK).

Objective: To determine the aetiology, clinical presentation and outcome of patients presenting with acute flaccid paralysis. Study Design: Cross-sectional study. Place and Duration of Study:

Background Fellowship programs offer training in a subspecialty focusing on distinct and advanced clinical/academic skills. This advanced postgraduate training allows physicians, who desire a more

Dr. Prem Chand is a distinguished Consultant Paediatric Neurologist and Epilepsy Specialist. Dr. Prem Chand completed his postgraduate training with honors from Aga Khan University

Neonatal seizures, Infantile & Childhood Epilepsies, Difficult to control Epilepsies, Genetic Epilepsies, Cerebral Palsy, Autism spectrum disorder, ADHD, Movement Disorder, Migraine Headaches, Meningitis & Encephalitis,

Viral encephalitis (VE) is an inflammation of the brain parenchyma caused by a viral infection. It presents with a range of neurological symptoms, including headache,

IntroductionGriscelli Syndrome (GS) is a rare autosomal recessive disorder characterized by immunodeficiency and partial albinism’. It results in pigmentary dilution of the skin and hair

The phenotypically similar genetic diseases Zimmermann-Laband syndrome (ZLS) and Temple-Baraitser syndrome (TMBTS) cause neurodevelopmental problems. Mutations in the gene coding for potassium voltage-gated channel, primarily

Pathological mutation of potassium channel subfamily T member 1 (KCNT1) gene causes an autosomal dominant disorder characterised by secondarily generalised seizures/migratory focal seizure, cyanosis, and

RPH3A encodes a protein involved in the stabilization of GluN2A subunit of NMDA-type glutamate receptors at the cell surface, forming a complex essential for synaptic

Asparagine-linked glycosylation thirteen (ALG13) gene-related congenital disorders of glycosylation (CDGs) include early onset epileptic encephalopathy (EIEE), developmental delays (DD) with intellectual disability (ID), speech and