Aicardi-Goutieres syndrome
MONDO:0018866Aicardi-Goutieres syndrome (AGS) is an inherited, subacute encephalopathy characterized by the association of basal ganglia calcification, leukodystrophy and cerebrospinal fluid (CSF) lymphocytosis.
Also known as: Aicardi Goutieres syndrome, Aicardi-Goutières Syndrome, Cree encephalitis, encephalopathy with basal ganglia calcification, encephalopathy with intracranial calcification and chronic lymphocytosis of cerebrospinal fluid, AGS, Aicardi-Goutières syndrome, encephalopathy, familial infantile, with calcification of basal ganglia and chronic cerebrospinal fluid lymphocytosis
110 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Aicardi-Goutieres syndrome 1
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Aicardi-Goutieres syndrome 2
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Aicardi-Goutieres syndrome 3
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Aicardi-Goutieres syndrome 4
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Aicardi-Goutieres syndrome 5
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Aicardi-Goutieres syndrome 6
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Aicardi-Goutieres syndrome 7
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Aicardi-Goutieres syndrome 8
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Aicardi-Goutieres syndrome 9
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Basal ganglia calcification, idiopathic, childhood-onset
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TREX1-related autosomal dominant Aicardi-Goutieres syndrome
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