B. Zilfalil

Infantile GM1 Gangliosidosis Presenting with Neuroregression and Leukodystrophy: A Case Report

GM1 gangliosidosis is a rare autosomal recessive lysosomal storage disorder caused by β-galactosidase deficiency, resulting in GM1 ganglioside accumulation. The infantile form presents early with developmental regression and hypotonia. We report a 20-month-old Malay girl with progressive neuroregression, macrocephaly,...

Strengthening legal safeguards against genetic discrimination: review and recommendations for Malaysia

Financing and health system capacity for precision medicine in Asia: a six country landscape analysis

Abstract Background Precision medicine (PM) adoption is accelerating across Asia, but implementation remains uneven due to differences in financing, infrastructure, governance, and health-system readiness. Objectives To examine how six Asian countries (Singapore, South Korea, China, Malaysia, Thailand, and Indonesia) a...