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About MLD (Metachromatic leukodystrophy)
Alternative Names:
MLD; Arylsulfatase A deficiency; Leukodystrophy - metachromatic
Definition of Metachromatic leukodystrophy:
Metachromatic leukodystrophy (MLD) is a genetic disorder that affects nerves, muscles, other organs, and behaviour. It slowly gets worse over time.

Causes, incidence, and risk factors:
MLD is usually caused by the lack of an important enzyme called arylsulfatase A. Because this enzyme is missing, chemicals called sulfatides build up in and damage the nervous system, kidneys, gallbladder, and other organs. In particular, the chemicals damage the protective sheaths that surround nerve cells.

The disease is passed down through families (inherited). You must get a copy of the defective gene from both your parents to have the disease. Parents can each have the defective gene, but not have MLD. A person with one defective gene is called a "carrier."
Children who inherit only one defective gene from one parent will be a carrier, but usually will not develop MLD. When two carriers have a child, there is a 25% chance that the child will get both genes and have MLD.

MLD occurs in about 1 in 40,000 people. There are three forms of the disease. They are based on when the symptoms begin:
Symptoms Metachromatic Leukodystrophy (MLD)?

> Late infantile MLD symptoms usually begin by ages 1 - 2.
> Juvenile MLD symptoms usually begin between ages 4 and 12.
> Adult (and latestage juvenile MLD) symptoms may occur between age 14 and      adulthood (over age 16), but may begin as late as the 40s or 50s.

Please visit MLD foundation for further information on this disease. Thank you for visiting this site and thank you for your kind donation.