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Canavan disease Health Article
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Definition
Canavan disease is an inherited condition that affects the breakdown and use (metabolism) of aspartic acid.
Alternative Names
Spongy degeneration of the brain; Aspartoacylase deficiency
Causes, incidence, and risk factors
Canavan disease is inherited as an autosomal recessive trait. It is more common among Ashkenazi Jews than in the general population. The lack of the enzyme, aspartoacylase, leads to a buildup of material called N-acetylaspartic acid in the brain. This causes the white matter of the brain to break down (deteriorate).
Symptoms
Symptoms usually begin in the first year of life. Parents tend to notice when a child is not reaching certain developmental milestones, including head control. Symptoms include:
Signs and tests
Tests:
Treatment
Treatment aims to ease the symptoms of the disease. There is no specific treatment.
Support Groups
Additional information and resources are available from: Canavan Foundation www.canavanfoundation.org 877-4-CANAVAN
Expectations (prognosis)
With Canavan disease, the central nervous system breaks down. Patients are likely to become disabled. Death often occurs before 18 months of age. However, some patients live until they are teenagers or, rarely, young adults.
Complications
This is often a fatal disorder. It includes severe disabilities such as:
Calling your health care provider
Call your health care provider if your child has any symptoms of Canavan disease. |
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