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Up to: Hereditary disorder of connective tissue · Autosomal recessive disease · Inborn error of immunity · Leukodystrophy · Type 1 interferonopathy of childhood

Aicardi-Goutieres syndrome

Aicardi-Goutieres syndrome (AGS) is an inherited, subacute encephalopathy characterized by the association of basal ganglia calcification, leukodystrophy and cerebrospinal fluid (CSF) lymphocytosis.

9 trials tagged with this condition →

  • Aicardi-Goutieres syndrome 1 2 trials Sub-types →
  • Aicardi-Goutieres syndrome 2 0 trials
  • Aicardi-Goutieres syndrome 3 0 trials
  • Aicardi-Goutieres syndrome 4 0 trials
  • Aicardi-Goutieres syndrome 5 0 trials
  • Aicardi-Goutieres syndrome 6 0 trials
  • Aicardi-Goutieres syndrome 7 0 trials
  • Aicardi-Goutieres syndrome 8 0 trials
  • Aicardi-Goutieres syndrome 9 0 trials
  • Basal ganglia calcification, idiopathic, childhood-onset 0 trials

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