53 top medical experts on Aicardi-Goutieres syndrome across 13 countries and 4 U.S. states, including 4 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Aicardi-Goutieres syndrome: Congenital intrauterine infection-like syndrome is characterised by the presence of microcephaly and intracranial calcifications at birth accompanied by neurological delay, seizures and a clinical course similar to that seen in patients after intrauterine infection with Toxoplasma gondii, Rubella, Cytomegalovirus, Herpes simplex (so-called TORCH syndrome), or other agents, despite repeated tests revealing the absence of any known infectious agent.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations

Organizations Providing General Support

  • Synonyms: Aicardi Goutieres syndrome,  Aicardi-Goutieres Syndrome 1,  Aicardi-Goutieres Syndrome 2,  Cree Encephalitis,  Encephalopathy with Basal Ganglia Calcification,  Familial Infantile Encephalopathy with Intracranial Calcification and Chronic Cerebrospinal Fluid Lymphocytosis,  Pseudo-TORCH syndrome,  Pseudotoxoplasmosis syndrome


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