Rasmussen syndrome and CNS granulomatous disease with NOD2/CARD15 mutations

Academic Article

Abstract

  • Rasmussen syndrome (RS) is a clinical diagnosis characterized by persistent focal seizures in a previously healthy child. Occasionally, the typical features of RS may be followed by another diagnosis. We discuss the course of a 12-year-old girl who presented with RS but was later diagnosed with CNS granulomatous disease and NOD2/CARD15 mutations. Her response to infliximab suggests that it should be included in immune-modulatory therapies used to treat these refractory disorders. ©2007AAN Enterprises, Inc.
  • Authors

    Published In

  • Neurology  Journal
  • Digital Object Identifier (doi)

    Author List

  • Goyal M; Cohen ML; Bangert BA; Robinson S; Singer NG
  • Start Page

  • 640
  • End Page

  • 643
  • Volume

  • 69
  • Issue

  • 7