Classic imaging features of L-2-hydroxyglutaric aciduria in young adult presenting as seizures associated with fever

L-2 Hydroxyglutaric aciduria is a rare metabolic disorder which is autosomal recessive in inheritance. It is characterised by the increased urinary excretion of L-2 hydroxyglutaric acid and the diagnosis is based on the increased levels of the L-2 hydroxy glutaric acid in the urine, serum & CSF....

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Bibliographic Details
Main Authors: Suresh Kumar, Shikha Bhatia, Mukesh Surya, Sanjiv Sharma
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2020-01-01
Series:Annals of Indian Academy of Neurology
Subjects:
Online Access:http://www.annalsofian.org/article.asp?issn=0972-2327;year=2020;volume=23;issue=3;spage=352;epage=354;aulast=