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Article

Early arteriopathy in Aicardi-Goutières syndrome 5. Case report and review of literature.

The neuroradiology journal - 1 Dec 2023

Markovic Ivana, Jocic-Jakubi Bosanka, Milenkovic Zoran

Abstract excerpt

Aicardi-Goutières syndrome (AGS) is an autosomal recessive disease that mimics congenital viral infection and mainly affects the brain, immune system, and skin. The dominant clinical symptom is the subacute onset of severe encephalopathy, which manifests as irritability, loss of ability, slowing of head growth, and poor nutrition. Arteriopathy in AGS is an uncommon manifestation usually associated with mutations...

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Identifiers

PMID: 36722173
DOI: 10.1177/19714009231154677
PMCID: PMC10649525

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