Natural course of glutamine synthetase deficiency in a 3 year old patient. uri icon

Overview

abstract

  • Glutamine deficiency with hyperammonemia due to an inherited defect of glutamine synthetase (GS) was found in a 2 year old patient. He presented neonatal seizures and developed chronic encephalopathy. Thus, GS deficiency leads to severe neurological disease but is not always early lethal.

publication date

  • February 4, 2011

Research

keywords

  • Brain Diseases, Metabolic
  • Glutamate-Ammonia Ligase

Identity

Scopus Document Identifier

  • 79955161364

Digital Object Identifier (DOI)

  • 10.1016/j.ymgme.2011.02.001

PubMed ID

  • 21353613

Additional Document Info

volume

  • 103

issue

  • 1