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Journal of Pediatric Epilepsy 2019; 08(02): 056-060
DOI: 10.1055/s-0039-1700838
DOI: 10.1055/s-0039-1700838
Case Report
Beyond the Phenotype: A Pediatric Case Series of Seizure and EEG Characteristics in Wolf-Hirschhorn Syndrome
Further Information
Publication History
22 April 2019
26 September 2019
Publication Date:
08 November 2019 (online)
Abstract
Wolf-Hirschhorn syndrome (WHS) is a rare genetic syndrome caused by deletion of a portion of the short arm of chromosome 4 (del 4p16.3). Aside from the many phenotypic abnormalities common in WHS, seizures are seen in the vast majority of the patients and are a potentially treatable cause of significant morbidity especially in the younger age group. Currently, however, little information is available regarding the associated seizure phenotypes, electroencephalographic (EEG) features, and seizure/epilepsy outcomes. This case series highlights the seizure phenotypes and EEG findings in three patients with WHS.
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References
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