Literature DB >> 28635494

Urea cycle disorder misdiagnosed as multiple sclerosis: a case report and review of the literature.

Hussein Algahtani1, Seham Alameer1, Yousef Marzouk2, Bader Shirah3.   

Abstract

Urea cycle disorders are a group of inborn errors of metabolism caused by dysfunction of any of the six enzymes or two transport proteins involved in urea biosynthesis. In this paper, we report a patient who presented with neurological dysfunction and coma in the immediate postpartum period. She was misdiagnosed for many years as a case of multiple sclerosis. The importance of reporting this case is to illustrate that the wrong diagnosis of patients as being affected with multiple sclerosis for many years due to magnetic resonance imaging abnormalities rather than the classic relapsing-remitting nature of the disease may lead to catastrophic consequences. The patient was treated with intravenous steroids several times, which is contraindicated in patients with urea cycle disorders as it may precipitate acute hyperammonemic attacks. In addition, the management of urea cycle disorder could have started earlier and avoided multiple admissions to the intensive care unit. We believe that the presence of symmetric hyperintense insular cortical changes are seen in multiple hyperammonemic processes, and in the context of the clinical presentation and high ammonia levels can be suggestive of a urea cycle disorder. For any patient presenting with atypical clinical features, images should be reviewed and discussed in detail with an experienced neuroradiologist. In addition, the ammonia levels should be checked if a urea cycle disorder is suspected.

Entities:  

Keywords:  MRI; Urea cycle disorder; misdiagnosis; multiple sclerosis; postpartum

Mesh:

Year:  2017        PMID: 28635494      PMCID: PMC5882056          DOI: 10.1177/1971400917715880

Source DB:  PubMed          Journal:  Neuroradiol J        ISSN: 1971-4009


  8 in total

Review 1.  Brain imaging in urea cycle disorders.

Authors:  Andrea Gropman
Journal:  Mol Genet Metab       Date:  2010-02-13       Impact factor: 4.797

Review 2.  Urea cycle disorders: a case report of a successful treatment with liver transplant and a literature review.

Authors:  Francesco Giuseppe Foschi; Maria Cristina Morelli; Sara Savini; Anna Chiara Dall'Aglio; Arianna Lanzi; Matteo Cescon; Giorgio Ercolani; Alessandro Cucchetti; Antonio Daniele Pinna; Giuseppe Francesco Stefanini
Journal:  World J Gastroenterol       Date:  2015-04-07       Impact factor: 5.742

Review 3.  Genotype-Phenotype Correlations in Ornithine Transcarbamylase Deficiency: A Mutation Update.

Authors:  Ljubica Caldovic; Iman Abdikarim; Sahas Narain; Mendel Tuchman; Hiroki Morizono
Journal:  J Genet Genomics       Date:  2015-05-19       Impact factor: 4.275

Review 4.  Neurologic damage and neurocognitive dysfunction in urea cycle disorders.

Authors:  Gregory M Enns
Journal:  Semin Pediatr Neurol       Date:  2008-09       Impact factor: 1.636

Review 5.  Neurological implications of urea cycle disorders.

Authors:  A L Gropman; M Summar; J V Leonard
Journal:  J Inherit Metab Dis       Date:  2007-11-23       Impact factor: 4.982

Review 6.  Hyperammonemia due to urea cycle disorders: a potentially fatal condition in the intensive care setting.

Authors:  Marcel Cerqueira Cesar Machado; Fabiano Pinheiro da Silva
Journal:  J Intensive Care       Date:  2014-03-13

7.  Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 cases.

Authors:  Elena Martín-Hernández; Luis Aldámiz-Echevarría; Esperanza Castejón-Ponce; Consuelo Pedrón-Giner; María Luz Couce; Juliana Serrano-Nieto; Guillem Pintos-Morell; Amaya Bélanger-Quintana; Mercedes Martínez-Pardo; María Teresa García-Silva; Pilar Quijada-Fraile; Isidro Vitoria-Miñana; Jaime Dalmau; Rosa A Lama-More; María Amor Bueno-Delgado; Mirella Del Toro-Riera; Inmaculada García-Jiménez; Concepción Sierra-Córcoles; Mónica Ruiz-Pons; Luis J Peña-Quintana; Inmaculada Vives-Piñera; Ana Moráis; Elena Balmaseda-Serrano; Silvia Meavilla; Pablo Sanjurjo-Crespo; Celia Pérez-Cerdá
Journal:  Orphanet J Rare Dis       Date:  2014-11-30       Impact factor: 4.123

8.  Guidelines for acute management of hyperammonemia in the Middle East region.

Authors:  Majid Alfadhel; Fuad Al Mutairi; Nawal Makhseed; Fatma Al Jasmi; Khalid Al-Thihli; Emtithal Al-Jishi; Moeenaldeen AlSayed; Zuhair N Al-Hassnan; Fathiya Al-Murshedi; Johannes Häberle; Tawfeg Ben-Omran
Journal:  Ther Clin Risk Manag       Date:  2016-03-31       Impact factor: 2.423

  8 in total
  2 in total

1.  MRI Findings in Acute Hyperammonemic Encephalopathy: Three Cases of Different Etiologies: Teaching Point: To recognize MRI findings in acute hyperammonemic encephalopathy.

Authors:  Elisabeth Reis; Tim Coolen; Valentina Lolli
Journal:  J Belg Soc Radiol       Date:  2020-01-30       Impact factor: 1.894

Review 2.  Contribution of Metabolomics to Multiple Sclerosis Diagnosis, Prognosis and Treatment.

Authors:  Marianna Gabriella Rispoli; Silvia Valentinuzzi; Giovanna De Luca; Piero Del Boccio; Luca Federici; Maria Di Ioia; Anna Digiovanni; Eleonora Agata Grasso; Valeria Pozzilli; Alessandro Villani; Antonio Maria Chiarelli; Marco Onofrj; Richard G Wise; Damiana Pieragostino; Valentina Tomassini
Journal:  Int J Mol Sci       Date:  2021-10-15       Impact factor: 5.923

  2 in total

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