John Libbey Eurotext

Epileptic Disorders

The Educational Journal of the International League Against Epilepsy

Mowat-Wilson syndrome presenting with fever-associated seizures Volume 19, numéro 4, December 2017

Illustrations

  • Figure 1
  • Figure 2

Tableaux

Auteurs
1 Division of Pediatric Neurology, Department of Pediatrics, Severance Children's Hospital, Yonsei University College of Medicine, Seoul
2 Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea
* Correspondence: Hoon-Chul Kang Division of Pediatric Neurology, Department of Pediatrics, Severance Children's Hospital, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul, 03722, Korea
a These authors contributed equally
  • Mots-clés : Mowat-Wilson syndrome, epilepsy, febrile seizure, next-generation sequencing, ZEB2
  • DOI : 10.1684/epd.2017.0949
  • Page(s) : 481-5
  • Année de parution : 2017

Mowat-Wilson syndrome (MWS) is a disorder caused by mutations or deletions of the zinc finger E-box-binding homeobox 2 (ZEB2) gene. Diagnosis of MWS can be challenging to neurologists, because its manifestations are diverse and the spectrum of genetic mutations are broad. Here, we describe two patients with MWS who initially showed atypical forms of fever-triggered seizures during childhood. Both had characteristic facial features, cognitive impairment, and genito-urinary anomalies consistent with MWS. By performing targeted next-generation sequencing (NGS) using a gene panel for epilepsy, we were able to identify a nonsense mutation (c.1965C>A) in the ZEB2 gene of one patient and a frameshift mutation (c.2348dupC) in the other patient. Fever-induced seizures can be presenting signs of MWS. MWS should be considered in the differential diagnosis of fever-induced seizures, especially when the patient has distinctive facial features and multiple anomalies, including cardiac, genito-urinary, and eye defects.