A Rare Case of Aicardi Goutieres Syndrome at TMCH - A Case report

Aicardi - Goutiere's syndrome is characterized by encephalopathy, developmental regression, acquired microcephaly, sterile pyrexia, seizures, chilblain, calcification of basal ganglia in CTMRI. It comes under a type of Autosomal Recessive Leukodystrophy usually presenting within first weeks of life and is generally fatal within first few years.