About The Medical Condition Canavan Disease, Type II
Find the definition of the medical term Canavan Disease, Type II. Canavan Disease, Type II defined and explained for easy understanding at the Medical Conditions from ClusterMed.info.
Canavan Disease, Type II
Canavan Disease, Type II Medical Condition |
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What's The Definition Of The Medical Condition Canavan Disease, Type II?
A rare neurodegenerative condition of infancy or childhood characterized by white matter vacuolization and demeylination that gives rise to a spongy appearance. Aspartoacylase deficiency leads to an accumulation of N-acetylaspartate in astrocytes. Inheritance may be autosomal recessive or the illness may occur sporadically. This illness occurs more frequently in individuals of Ashkenazic Jewish descent. The neonatal form features the onset of hypotonia and lethargy at birth, rapidly progressing to coma and death. The infantile form features developmental delay, DYSKINESIAS, hypotonia, spasticity, blindness, and megalencephaly. The juvenile form is characterized by ATAXIA; OPTIC ATROPHY; and DEMENTIA. (From Adams et al., Principles of Neurology, 6th ed, p944; Am J Med Genet 1988 Feb;29(2):463-71)
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