Objectives Considering the dearth of literature on West syndrome (WS) from South Asian
countries, this study aimed to evaluate the management practices in South Asia by an online …

Purpose This study was intended to document the clinical profile and treatment outcome of
West syndrome in children attending a tertiary care center in Northern India. Method Data …

This study describes the clinical characteristics, treatment, and outcome of children with
West syndrome in a tertiary care hospital in north India. Overall, 310 case records diagnosed …

Objective To determine epilepsy and neurodevelopmental outcomes beyond 2 y of age and
their putative prognostic factors in children with West syndrome (WS). Methods This cross …

Objectives Long‐term adrenocorticotropic therapy (LT‐ACTH), which consisted of 2‐4
weeks of daily injections of adrenocorticotropic hormone (ACTH) and subsequent months of …

West syndrome is one of the most refractory epileptic syndromes in infancy, and many
researchers have made great effort to find optimal treatment modalities for this syndrome. In …

OBJECTIVES: To determine the dosage and factors influencing efficacy of
adrenocorticotropic hormone (ACTH) for West syndrome. STUDY DESIGN: A retrospective …

Justification West syndrome is one of the commonest causes of epilepsy in infants and
young children and is a significant contributor to neurodevelopmental morbidity. Multiple …

Objectives: To assess the neurodevelopmental outcome of West syndrome (WS) in Indian
children, who differ in their clinical profile from the western population. Materials and …

Purpose Nearly half of all patients with seizure onset in the first year of life suffer from West
syndrome (WS). The prognosis of epilepsy and psychosocial outcomes in children with WS …