Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8690574 | Pediatric Neurology | 2017 | 22 Pages |
Abstract
In addition to the well-described epileptic encephalopathy, pyridox(am)ine 5â²-phosphate oxidase deficiency causes a range of neurological and systemic manifestations. A movement disorder, developmental delay, and encephalopathy, as well as retinopathy, anemia, and failure to thrive add to the broadening clinical spectrum of P5P dependent epilepsy.
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Authors
Réjean M. DO, Archana A. MD, MPH, Brian MD, Fiona M. MD, Ankoor S. MD, Jurriaan M. MD, Lance H. MD, Pankaj B. MBBS, MMSc, Phillip L. MD, Masanori MD,