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Article

Rasmussen syndrome and CNS granulomatous disease with NOD2/CARD15 mutations.

Neurology - 14 Aug 2007

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

Abstract excerpt

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 C...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17698784
DOI: 10.1212/01.wnl.0000267429.89675.03

Genes

NOD2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17698784-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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