Canavan diseaseSpongy degeneration of the brain; Aspartoacylase deficiency; Canavan - van Bogaert disease
Canavan disease is a condition that affects how the body breaks down and uses aspartic acid.
Aspartic acid is a nonessential amino acid. Amino acids are building blocks of proteins. "Nonessential" means that our bodies produce it, even if we...Read Article Now Book Mark Article
Canavan disease is passed down (inherited) through families. It is more common among the Ashkenazi Jewish population 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.
White matter of the brain
White matter is found in the deeper tissues of the brain (subcortical). It contains nerve fibers (axons), which are extensions of nerve cells (neuro...Read Article Now Book Mark Article
There are two forms of the disease:
- Neonatal (infantile) -- This is the most common form. Symptoms are severe. Babies seem to be normal the first few months after birth. By 3 to 5 months, they have developmental problems, such as those mentioned below under the Symptoms section of this article.
- Juvenile -- This is a less common form. Symptoms are mild. Developmental problems are less severe than those of the neonatal form. In some cases, the symptoms are so mild that they go undiagnosed as Canavan disease.
Symptoms often begin in the first year of life. Parents tend to notice it when their child is not reaching certain developmental milestones, including head control.
- Abnormal posture with flexed arms and straight legs
- Food material flows back into the nose
- Feeding problems
- Increasing head size
- Poor muscle tone, especially of the neck muscles
- A lack of head control when baby is pulled from a lying to a sitting position
- Poor visual tracking, or blindness
- Reflux with vomiting
- Severe intellectual disability
- Swallowing difficulties
Exams and Tests
A physical exam may show:
- Exaggerated reflexes
- Joint stiffness
- Loss of tissue in the optic nerve of the eye
Tests for this condition include:
- Blood chemistry
- CSF chemistry
- Genetic testing for aspartoacylase gene mutations
- Head CT scan
- Head MRI scan
- Urine or blood chemistry for elevated aspartic acid
- DNA analysis
There is no specific treatment available. Supportive care is very important to ease the symptoms of the disease. Lithium and gene therapy are being studied.
The following resources can provide more information on Canavan disease:
- National Organization for Rare Disorders -- rarediseases.org/rare-diseases/canavan-disease
- National Tay-Sachs & Allied Diseases Association -- www.ntsad.org/index.php/the-diseases/canavan
With Canavan disease, the central nervous system breaks down. People are likely to become disabled.
Central nervous system
The central nervous system is composed of the brain and spinal cord. Your brain and spinal cord serve as the main "processing center" for your entir...Read Article Now Book Mark Article
Those with the neonatal form often do not live beyond childhood. Some children may live into their teens. Those with the juvenile form often live a normal lifespan.
This disorder nay cause severe disabilities such as:
- Inability to walk
- Intellectual disability
When to Contact a Medical Professional
Call your health care provider if your child has any symptoms of Canavan disease.
Genetic counseling is recommended for people who want to have children and have a family history of Canavan disease. Counseling should be considered if both parents are of Ashkenazi Jewish descent. For this group, DNA testing can almost always tell if the parents are carriers.
A diagnosis may be made before the baby is born (prenatal diagnosis) by testing the amniotic fluid, the fluid that surrounds the womb.
Amniotic fluid is a clear, slightly yellowish liquid that surrounds the unborn baby (fetus) during pregnancy. It is contained in the amniotic sac....Read Article Now Book Mark Article
Elitt CM, Volpe JJ. Degenerative disorders of the newborn. In: Volpe JJ, Inder TE, Darras BT, et al, eds. Volpe's Neurology of the Newborn. 6th ed. Philadelphia, PA: Elsevier; 2018:chap 29.
Matalon RK, Trapasso JM. Defects in metabolism of amino acids: N-acetylaspartic acid (Canavan disease). In: Kliegman RM, St. Geme JW, Blum NJ, Shah SS, Tasker RC, Wilson KM, eds. Nelson Textbook of Pediatrics. 21st ed. Philadelphia, PA: Elsevier; 2020:chap 103.15.
Vanderver A, Wolf NI. Genetic and metabolic disorders of the white matter. In: Swaiman KF, Ashwal S, Ferriero DM, et al, eds. Swaiman's Pediatric Neurology: Principles and Practice. 6th ed. Philadelphia, PA: Elsevier; 2017:chap 99.
Review Date: 10/3/2019
Reviewed By: Anna C. Edens Hurst, MD, MS, Assistant Professor in Medical Genetics, The University of Alabama at Birmingham, Birmingham, AL. Review provided by VeriMed Healthcare Network. Also reviewed by David Zieve, MD, MHA, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team.