Article ID Journal Published Year Pages File Type
3084726 Pediatric Neurology 2015 4 Pages PDF
Abstract
This child's unusual acute presentation, along with his prolonged mild course, raises questions about the relationship between biochemical signs of abnormal aspartoacylase function and clinical findings. This patient highlights the need for long-term clinical follow-up of children with mild Canavan disease to clarify the significance of these biochemical abnormalities.
Related Topics
Life Sciences Neuroscience Developmental Neuroscience
Authors
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