Literature DB >> 3661651

Transient visual loss in ornithine transcarbamoylase deficiency.

N G Snebold1, J F Rizzo, S Lessell, R C Pruett.   

Abstract

We examined a 32-year-old, previously healthy man who developed episodic bilateral visual impairment and confusion. Coincident hyperammonemia led to the diagnosis of ornithine transcarbamoylase deficiency, which was established by enzymatic analysis of a liver biopsy specimen. The available data were insufficient to determine if the metabolic derangement impaired vision at the level of the optic nerves or at the cerebral level.

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Year:  1987        PMID: 3661651     DOI: 10.1016/0002-9394(87)90232-7

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  7 in total

1.  Ornithine carbamoyltransferase deficiency: unusual clinical findings and novel mutation.

Authors:  V E Shih; A P Safran; A H Ropper; M Tuchman
Journal:  J Inherit Metab Dis       Date:  1999-06       Impact factor: 4.982

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.  Rapidly fatal hyperammonemic coma in adults. Urea cycle enzyme deficiency.

Authors:  B E Wilson; W N Hobbs; J J Newmark; S J Farrow
Journal:  West J Med       Date:  1994-08

4.  Transient Cortical Blindness in a Toddler With Heterozygous Ornithine Transcarbamylase Deficiency.

Authors:  Peter N Eskander; Sara S Romani
Journal:  Cureus       Date:  2021-11-30

Review 5.  Suggested guidelines for the diagnosis and management of urea cycle disorders.

Authors:  Johannes Häberle; Nathalie Boddaert; Alberto Burlina; Anupam Chakrapani; Marjorie Dixon; Martina Huemer; Daniela Karall; Diego Martinelli; Pablo Sanjurjo Crespo; René Santer; Aude Servais; Vassili Valayannopoulos; Martin Lindner; Vicente Rubio; Carlo Dionisi-Vici
Journal:  Orphanet J Rare Dis       Date:  2012-05-29       Impact factor: 4.123

6.  Multimodal imaging in urea cycle-related neurological disease - What can imaging after hyperammonemia teach us?

Authors:  Kuntal Sen; Matthew T Whitehead; Andrea L Gropman
Journal:  Transl Sci Rare Dis       Date:  2020-08-03

7.  Cross-sectional observational study of 208 patients with non-classical urea cycle disorders.

Authors:  Corinne M Rüegger; Martin Lindner; Diana Ballhausen; Matthias R Baumgartner; Skadi Beblo; Anibh Das; Matthias Gautschi; Esther M Glahn; Sarah C Grünert; Julia Hennermann; Michel Hochuli; Martina Huemer; Daniela Karall; Stefan Kölker; Robin H Lachmann; Amelie Lotz-Havla; Dorothea Möslinger; Jean-Marc Nuoffer; Barbara Plecko; Frank Rutsch; René Santer; Ute Spiekerkoetter; Christian Staufner; Tamar Stricker; Frits A Wijburg; Monique Williams; Peter Burgard; Johannes Häberle
Journal:  J Inherit Metab Dis       Date:  2013-06-19       Impact factor: 4.982

  7 in total

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