A case of juvenile Canavan disease with distinct pons involvement

Canavan disease is a genetic neurodegenerative leukodystrophy that results in the spongy degeneration of the white matter. Its key clinical features in the infantile form are developmental delay, visual problems and macrocephaly. Congenital and juvenile forms have also been described.
Source: Brain and Development - Category: Neurology Authors: Tags: Case Report Source Type: research