All types of leukodystrophy are genetic (present at conception), progressive, and never spontaneously resolve. None of the leukodystrophies can be cured, and effective treatments are limited.
Canavan disease in Ashkenazi Jews, or globoid cell leukodystrophy (GLD) and metachromatic leukodystrophy (MLD) in Scandinavians.
They are all caused by either an abnormality in one of the protein components of myelin, or by a defective or missing enzyme that assists in the production or normal degradation of myelin
Einstin
The juvenile form of metachromatic leukodystrophy is characterized by gait disturbances, urinary incontinence, mental deterioration, and emotional difficulties
It was incorporated in 1982
they occur in the brain
I am not sure... Although, I suffer majorly from Hemi-Hyper Trophy. I am 13. It is very hard to deal with. Do you have Leukodystrophy oh Hemi-Hyper Trophy?
Metachromatic leukodystrophy (MLD) is a rare degenerative neurological disease affecting the fatty covering that acts as an insulator around nerve fibers known as the myelin sheath.
People are diagnosed with leukodystrophy through a combination of clinical evaluation, imaging studies, and genetic testing. A neurologist typically assesses symptoms such as motor difficulties or cognitive decline, followed by brain imaging techniques like MRI to identify characteristic changes in white matter. Genetic testing is then conducted to confirm the diagnosis and identify specific mutations associated with different types of leukodystrophy. Blood tests and sometimes cerebrospinal fluid analysis may also be used to rule out other conditions.
Liver and kidney falure.
Adult metachromatic leukodystrophy is characterized by emotional disturbances and psychiatric symptoms. Disorders of movement and posture appear later. Dementia and decreased visual function also occur.
Metachromatic leukodystrophy (MLD), also called sulfatide lipidosis and arylsulfatase A (ARSA) deficiency, is inherited as an autosomal recessive trait, due to mutations in the arylsulfatase A (ARSA) gene