Successful corpus callosotomy for post-encephalopathic refractory epilepsy in a patient with MECP2 duplication syndrome
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health
Reference12 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999
2. Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy;Lugtenberg;Eur J Hum Genet,2009
3. The MECP2 duplication syndrome;Ramocki;Am J Med Genet A,2010
4. Neurologic aspects of MECP2 gene duplication in male patients;Echenne;Pediatr Neurol,2009
5. Expanding the clinical picture of the MECP2 duplication syndrome;Lim;Clin Genet,2017
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1. Surgical outcomes of patients with genetically refractory epilepsy: A systematic review and meta-analysis;Seizure: European Journal of Epilepsy;2024-08
2. How Families Manage the Complex Medical Needs of Their Children with MECP2 Duplication Syndrome;Children;2023-07-11
3. A brief history of MECP2 duplication syndrome: 20-years of clinical understanding;Orphanet Journal of Rare Diseases;2022-03-21
4. Molecular and clinical insights into complex genomic rearrangements related to MECP2 duplication syndrome;European Journal of Medical Genetics;2021-12
5. MECP2-Related Disorders in Males;International Journal of Molecular Sciences;2021-09-04
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