Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3084726 | Pediatric Neurology | 2015 | 4 Pages |
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.
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Authors
Katherine E. BA, Stephen F. MD, Bryan E. MD, PhD, Meredith R. MD, MSc,