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Results 1 - 7 of 9 for Aicardi Goutieres syndrome 2
  1. ... RNASEH2A gene have been identified in people with Aicardi-Goutières syndrome, a disorder that involves severe brain dysfunction (encephalopathy), ... system activation. The RNASEH2A gene mutations that cause Aicardi-Goutières syndrome likely result in a dysfunctional RNase H2 complex. ...
  2. ... TREX1 gene have been identified in people with Aicardi-Goutières syndrome, a disorder that involves severe brain dysfunction (encephalopathy), ... and result in the signs and symptoms of Aicardi-Goutières syndrome. More About This Health Condition Mutations in the ...
  3. ... SAMHD1 gene have been identified in people with Aicardi-Goutières syndrome, a disorder that involves severe brain dysfunction (encephalopathy), ... systems that lead to the characteristic features of Aicardi-Goutières syndrome. More About This Health Condition AGS5 DCIP dendritic ...
  4. ... gene mutations have been found in people with Aicardi-Goutières syndrome. This disorder is characterized by abnormalities of the ... the brain.The IFIH1 gene mutations involved in Aicardi-Goutières syndrome are described as "gain-of-function" because they ...
  5. ... gene mutations have been identified in people with Aicardi-Goutières syndrome, a disorder that involves severe brain dysfunction (encephalopathy), ... organs, leading to the signs and symptoms of Aicardi-Goutières syndrome. More About This Health Condition More than 180 ...
  6. ... pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutieres syndrome. Eur J Paediatr Neurol. 2016 Jul;20(4): ...
  7. ... 22. Citation on PubMed Fertleman CR, Ferrie CD, Aicardi J, Bednarek NA, ... Brain. 2012 Feb;135(Pt 2):313-6. doi: 10.1093/brain/aws007. No ...