Research Article | Open Access
Case Report on Late Infantile Type Metachromatic Leukodystrophy
Ms. Chitra G. Wanjari Ms. Shital Sakharkar Aniket Pathade
Pages: 7699-7701
Abstract
Background: Metachromatic leukodystrophy is a genetic disorder characterized by the accumulation of fatty substances (lipids) in cells, particularly in the brain, spinal cord, and peripheral nerves. A lack of sulfatides,which are enzymes that aid in the breakdown of lipids, causes this buildup. The brain and nervous system gradually lose function as the substance that covers and protects nerve cells (myelin) is damaged
Keywords
Metachromatic leukodystrophy, Arylsulfatase, Periventricular