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Article

Aicardi-Goutières syndrome (AGS).

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society - 1 Sept 2008

Stephenson John B P

Abstract excerpt

In 1984, Jean Aicardi and Françoise Goutières described 8 children showing both severe brain atrophy and chronic cerebrospinal fluid lymphocytosis, with basal ganglia calcification in at least one member of each affected family. The course was rapid to death or a vegetative outcome. Aicardi and Goutières correctly predicted that the disorder would be genetic, but emphasised that "some features, especially the...

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Source

Identifiers

PMID: 18343173
DOI: 10.1016/j.ejpn.2007.11.010

Genes

TREX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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