Recurrent encephalopathy with spinal cord involvement: An atypical manifestation of Aicardi–Goutières syndrome

Recurrent encephalopathy with spinal cord involvement: An atypical manifestation of Aicardi–Goutières syndrome

Aicardi–Goutières syndrome (AGS) is a rare, genetic inflammatory disease due to mutations in any of the seven genes discovered to date (TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1). Clinical onset is seen most commonly in utero or in infancy; irritability, feeding difficulties, jitt...

Full description

Bibliographic Details
Main Authors: Debopam Samanta, Raghu Ramakrishnaiah
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Annals of Indian Academy of Neurology
Subjects:
Acute necrotizing encephalopathy
ADAR mutation
Aicardi–Goutières syndrome
dyschromatosis symmetrica hereditaria
influenza encephalopathy
Online Access:http://www.annalsofian.org/article.asp?issn=0972-2327;year=2019;volume=22;issue=1;spage=111;epage=115;aulast=Samanta

Internet

http://www.annalsofian.org/article.asp?issn=0972-2327;year=2019;volume=22;issue=1;spage=111;epage=115;aulast=Samanta

Similar Items