Rasmussen syndrome and CNS granulomatous disease with NOD2/CARD15 mutations

M. Goyal; M. L. Cohen; B. A. Bangert; S. Robinson; N. G. Singer

doi:10.1212/01.wnl.0000267429.89675.03

Rasmussen syndrome and CNS granulomatous disease with NOD2/CARD15 mutations

M. Goyal, M. L. Cohen, B. A. Bangert, S. Robinson, N. G. Singer

Research output: Contribution to journal › Article › peer-review

6 Scopus citations

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.

Original language	English (US)
Pages (from-to)	640-643
Number of pages	4
Journal	Neurology
Volume	69
Issue number	7
DOIs	https://doi.org/10.1212/01.wnl.0000267429.89675.03
State	Published - Aug 2007
Externally published	Yes

ASJC Scopus subject areas

Clinical Neurology

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AU - Goyal, M.

AU - Cohen, M. L.

AU - Bangert, B. A.

AU - Robinson, S.

AU - Singer, N. G.

PY - 2007/8

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AB - 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.

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Rasmussen syndrome and CNS granulomatous disease with NOD2/CARD15 mutations

Abstract

ASJC Scopus subject areas

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