Literature DB >> 33552645

Expanding Role of Proton Magnetic Resonance Spectroscopy: Timely Diagnosis and Treatment Initiation in Partial Ornithine Transcarbamylase Deficiency.

Kuntal Sen1, Carlos Castillo Pinto2, Andrea L Gropman1.   

Abstract

We report the case of a 3-year-old male patient who presented with a 3-day history of altered mental status, emesis, and abdominal pain in the setting of a viral illness. A rapid screening revealed a high ammonia level and after reviewing his proton magnetic resonance spectroscopy (1H MRS) which showed the classic triad of high glutamate, low choline, and myoinositol, a diagnosis of ornithine transcarbamylase deficiency (OTCD) was made within 6 hours of presentation. Therapy with sodium phenylbutyrate and sodium benzoate was initiated and patient was discharged after 3 days with no neurologic disability. Biochemical and molecular testing eventually confirmed the diagnosis. 1H MRS is a practical and fast neuroimaging modality that can aid in diagnosis of OTCD and enables faster initiation of treatment in acute settings. Thieme. All rights reserved.

Entities:  

Keywords:  multimodal neuroimaging; partial OTC deficiency; proton MR spectroscopy

Year:  2020        PMID: 33552645      PMCID: PMC7853912          DOI: 10.1055/s-0040-1709670

Source DB:  PubMed          Journal:  J Pediatr Genet        ISSN: 2146-460X


  18 in total

Review 1.  Imaging of neurogenetic and neurometabolic disorders of childhood.

Authors:  Andrea Gropman
Journal:  Curr Neurol Neurosci Rep       Date:  2004-03       Impact factor: 5.081

2.  Estimated frequency of urea cycle enzymopathies in Japan.

Authors:  N Nagata; I Matsuda; K Oyanagi
Journal:  Am J Med Genet       Date:  1991-05-01

Review 3.  Inborn errors of metabolism.

Authors:  Ayman W El-Hattab
Journal:  Clin Perinatol       Date:  2015-04-08       Impact factor: 3.430

4.  Mutations and polymorphisms in the human ornithine transcarbamylase (OTC) gene.

Authors:  Saori Yamaguchi; Lisa L Brailey; Hiroki Morizono; Allen E Bale; Mendel Tuchman
Journal:  Hum Mutat       Date:  2006-07       Impact factor: 4.878

Review 5.  Mutations and polymorphisms in the human ornithine transcarbamylase gene.

Authors:  Mendel Tuchman; Naser Jaleel; Hiroki Morizono; Lisa Sheehy; Michael G Lynch
Journal:  Hum Mutat       Date:  2002-02       Impact factor: 4.878

6.  An integrated approach to the diagnosis and prospective management of partial ornithine transcarbamylase deficiency.

Authors:  Fernando Scaglia; Qiping Zheng; William E O'Brien; Joseph Henry; Judy Rosenberger; Peter Reeds; Brendan Lee
Journal:  Pediatrics       Date:  2002-01       Impact factor: 7.124

7.  1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency.

Authors:  A L Gropman; S T Fricke; R R Seltzer; A Hailu; A Adeyemo; A Sawyer; J van Meter; W D Gaillard; R McCarter; M Tuchman; M Batshaw
Journal:  Mol Genet Metab       Date:  2008-07-26       Impact factor: 4.797

8.  Neonatal case of classic maple syrup urine disease: usefulness of (1) H-MRS in early diagnosis.

Authors:  Takeshi Sato; Koji Muroya; Junko Hanakawa; Yumi Asakura; Noriko Aida; Moyoko Tomiyasu; Go Tajima; Tomonobu Hasegawa; Masanori Adachi
Journal:  Pediatr Int       Date:  2014-02       Impact factor: 1.524

Review 9.  Neuroimaging in mitochondrial disorders.

Authors:  Andrea L Gropman
Journal:  Neurotherapeutics       Date:  2013-04       Impact factor: 7.620

10.  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
View more
  3 in total

Review 1.  Fifteen years of urea cycle disorders brain research: Looking back, looking forward.

Authors:  Kuntal Sen; Matthew Whitehead; Carlos Castillo Pinto; Ljubica Caldovic; Andrea Gropman
Journal:  Anal Biochem       Date:  2021-10-09       Impact factor: 3.365

Review 2.  Neuromonitoring in Rare Disorders of Metabolism.

Authors:  Carlos Castillo-Pinto; Kuntal Sen; Andrea Gropman
Journal:  Yale J Biol Med       Date:  2021-12-29

Review 3.  Dysregulation of Astrocytic Glutamine Transport in Acute Hyperammonemic Brain Edema.

Authors:  Magdalena Zielińska; Jan Albrecht; Mariusz Popek
Journal:  Front Neurosci       Date:  2022-06-06       Impact factor: 5.152

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.