BACKGROUND AND PURPOSE: To date, few studies have focused specifically on imaging
findings in Aicardi-Goutières syndrome (AGS). We set out to evaluate retrospectively …

The International Aicardi-Goutières Syndrome Association (IAGSA) was founded in 2000, its
aim being to collect and analyse all available information on this rare syndrome (whose true …

Aim: To describe the clinical and neuroimaging findings in new cases with Aicardi‐Goutières
syndrome (AGS) from Egypt. Methods: Ten patients with progressive encephalopathy …

Aicardi-Goutières syndrome is a severe and progressive familial encephalopathy that is
characterized by acquired microcephaly, intracranial calcification (mainly of the basal …

We report 2 siblings with the Aicardi-Goutières syndrome (encephalopathy, basal ganglia
calcifications, and persistent cerebrospinal fluid pleiocytosis). The eldest sibling is severely …

Abstract The Aicardi-Goutières syndrome (ACS) is an autosomal recessive progressive
encephalopathy associated with basal ganglia calcification, white-matter abnormality …

Objective: To perform an updated characterization of the neuroradiologic features of Aicardi-
Goutières syndrome (AGS). Methods: The neuroradiologic data of 121 subjects with AGS …

Described are the outcomes of 11 Italian patients with Aicardi–Goutières syndrome.
Neurologic symptoms progressed in the first year of life and stabilized by the end of the …

Aicardi-Goutières syndrome (AGS)(McKusick 225750) is an autosomal recessive disease
with onset in the 1st year of life, resulting in progressive microcephaly, calcification of …

Abstract Background Aicardi-Goutières syndrome (AGS) is a genetic interferonopathy
characterized by early onset of severe neurological injury with intracranial calcifications …