Metachromatic Leukodystrophy information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
Metachromatic leukodystrophy is an inherited disorder characterized by the accumulation of fats called sulfatides in cells. This accumulation especially ...
Enzymes are proteins that help break down (metabolize) substances in the body. If certain enzymes are not present, the body will be unable to metabolize a substance.
Metachromatic leukodystrophy (MLD) is part of a larger group of lysosomal storage diseases, some of which are progressive, inherited, and neurodegenerative ...
Metachromatic leukodystrophy (MLD, also called Arylsulfatase A deficiency) is a lysosomal storage disease which is commonly listed in the family of leukodystrophies ...
Metachromatic leukodystrophy — Learn more about diagnosis and treatment at Mayo Clinic.
Leukodystrophy, Metachromatic. Important It is possible that the main title of the report Leukodystrophy, ... Late-Onset Metachromatic Leukodystrophy; ARSA;
Information, support, education and on-line networking for families throughout the world dealing with Metachromatic Leukodystrophy (MLD).
Metachromatic Leukodystrophy information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
Metachromatic leukodystrophy (MLD) is a genetic disorder that affects nerves, muscles, other organs, and behavior. It slowly gets worse over time.