Literature DB >> 8957809

CT and MRI in a girl with late-onset ornithine transcarbamylase deficiency: case report.

S K Bajaj1, G Kurlemann, G Schuierer, P E Peters.   

Abstract

We report CT and MRI findings in a girl with late-onset ornithine transcarbamylase deficiency, who presented with progressive somnolence. Both imaging methods showed signs of an acute cerebral ischaemia with new defects on follow-up. Despite an unusual clinical presentation, laboratory studies led to the diagnosis of this rare inherited metabolic defect.

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Year:  1996        PMID: 8957809     DOI: 10.1007/s002340050351

Source DB:  PubMed          Journal:  Neuroradiology        ISSN: 0028-3940            Impact factor:   2.804


  4 in total

1.  Neurological outcome of patients with ornithine carbamoyltransferase deficiency.

Authors:  P Nicolaides; D Liebsch; N Dale; J Leonard; R Surtees
Journal:  Arch Dis Child       Date:  2002-01       Impact factor: 3.791

2.  Urea cycle disorders: brain MRI and neurological outcome.

Authors:  William R Bireley; Johan L K Van Hove; Renata C Gallagher; Laura Z Fenton
Journal:  Pediatr Radiol       Date:  2011-10-12

3.  Brain MR imaging in neonatal hyperammonemic encephalopathy resulting from proximal urea cycle disorders.

Authors:  Jun-ichi Takanashi; A James Barkovich; Sabrina F Cheng; Kara Weisiger; Carol O Zlatunich; Christine Mudge; Philip Rosenthal; Mendel Tuchman; Seymour Packman
Journal:  AJNR Am J Neuroradiol       Date:  2003 Jun-Jul       Impact factor: 3.825

4.  Brain MR imaging in acute hyperammonemic encephalopathy arising from late-onset ornithine transcarbamylase deficiency.

Authors:  Jun-Ichi Takanashi; A James Barkovich; Sabrina F Cheng; Dana Kostiner; John C Baker; Seymour Packman
Journal:  AJNR Am J Neuroradiol       Date:  2003-03       Impact factor: 3.825

  4 in total

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