Early-Onset Epileptic Encephalopathy with Phospholipase C Beta 1 Deficiency
Abstract
The clinical presentation and evolution of epileptic encephalopathy associated with a loss-of-function mutation in the phospholipase C-b 1 gene are reported in a male infant with infantile spasms treated at the University of Birmingham School of Medicine, UK.
DOI: https://doi.org/10.15844/pedneurbriefs-24-12-2 | Journal eISSN: 2166-6482
Language: English
Page range: 90 - 91
Published on: Dec 1, 2010
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2010 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.