Leukodystrophy is a break down of a part of the brain called the myelin, which is also called white matter. Myelin protects the part of the nerve that sends signals from the brain to the rest of the body. The break down of myelin makes it difficult for the brain to send signals to the body. Leukodystrophy is a rare disease.
Types of leukodystrophies include:
- Metachromatic leukodystrophy
- Krabbé disease
- Pelizaeus-Merzbacher disease
- Canavan disease
- Childhood ataxia with central nervous system hypomyelination (CACH), which is also called vanishing white matter disease
- Alexander disease
- Refsum disease
- Cerebrotendinous xanthomatosis
Most leukodystrophies begin in infancy or childhood. However, there are several types that may not begin until adolescence or early adulthood.
Neuronal Axon With Myelin Sheath
Copyright © Nucleus Medical Media, Inc.
Leukodystrophy is caused by a genetic defect. This defect impairs the growth or development of the myelin. Each type of leukodystrophy is the result of a specific genetic defect. Most leukodystrophies are passed from parent to child, though some may develop freely.
A family history of leukodystrophy may increase your chance of leukodystrophy.
Symptoms of leukodystrophy may include:
- Gradual decline of the health of an infant or child who previously appeared well
- Loss or increase in muscle tone
- Change in movements
- Abnormal eye movements
- Change in walking pattern
- Loss of speech
- Loss of the ability to eat
- Loss of vision
- Loss of hearing
- Change in behavior
- Slowdown of mental and physical development
Some leukodystrophies may involve other organ systems which can cause:
- Heart disease
- Enlargement of the liver and spleen
- Skeletal abnormalities, such as short stature, coarse facial appearance, and joint stiffness
- Respiratory disease leading to breathing problems
- Bronzing of the skin
- Cholesterol nodules to form on tendons
Your doctor will ask about your symptoms and medical history. A physical exam will be done.
Images of the brain may be taken. This can be done with:
Your bodily fluids and tissues may be tested. This can be done with:
Tests may be done on your nerves. This can be done with:
Talk with your doctor about the best treatment plan for you. Treatment options include:
Depending on the type of leukodystrophy and the symptoms, treatment may include:
- Medications to reduce symptoms and relieve pain.
- Physical, occupational, and/or speech therapy
- Nutritional programs
- Recreational programs
In a few of the leukodystrophies,
bone marrow transplant
may help. It may be able to slow or stop the progression of the disease.
Replacement of the abnormal or absent enzyme is being explored for a few of the leukodystrophies. Research is being done in this area.
Talk to your doctor to find out what treatments may be right for you.
There is no known way to prevent leukodystrophy. For parents who have had a child with leukodystrophy, genetic counseling may be helpful. This counseling will help to determine the chances of having another child with the disease.
DeKosky S, Kaufer D, Hamilton R, Wolk D, Lopez O. The dementias. In: Bradley WG, ed.
Neurology in Clinical Practice.
5th ed. Philadelphia, PA: Butterworth Heinemann Elsevier; 2008.
Genotype and protein expression after bone marrow transplantation for adrenoleukodystrophy.
Arch Neurol. 2007;64:651-657.
Lamari F, et al. Disorders of phospholipids, sphingolibids, and fatty acids biosynthesis: toward a new category of inherited metabolic diseases.
J Inherit metab Dis. 2012. July 20.
Leukodystrophy information page. National Institute of Neurological Disorders and Stroke website. Available at:
. Updated May 6, 2010. Accessed May 20, 2013.
Metachromatic leukodystrophy. EBSCO DynaMed website. Available at:
. Updated January 20, 2011. Accessed May 20, 2013.
Moser HW, Mahmood A, Raymond GV.
X-linked adrenoleukodystrophy [review].
Nat Clin Pract Neurol. 2007;3:140-151.
Ropper AH, Brown RH.
Adams and Victor's Principles of Neurology. 8th ed. New York, NY: McGraw-Hill Medical Publishing Division; 2005: chap 37.
Shimozawa N. Molecular and clinical aspects of peroxisomal diseases [review].
J Inherit Metab Dis. 2007;30:193-197.
What is leukodystrophy? United Leukodystrophy Foundation website. Available at:
. Accessed May 20, 2013.
Last reviewed May 2013 by Rimas Lukas, MD; Michael Woods, MD
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
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