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Psychiatric adult-onset of urea cycle disorders: A case-series
Adult onset urea cycle disorders (UCD) may present with psychiatric symptoms, occasionally as the initial presentation. We aimed to describe the characteristics of patients presenting with a psychiatric adult-onset of UCDs, to discuss which signs could suggest this diagnosis in such a situation, and...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502717/ https://www.ncbi.nlm.nih.gov/pubmed/28725569 http://dx.doi.org/10.1016/j.ymgmr.2017.07.001 |
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author | Bigot, Adrien Brunault, Paul Lavigne, Christian Feillet, François Odent, Sylvie Kaphan, Elsa Thauvin, Christel Leguy, Vanessa Broué, Pierre Tchan, Michel C. Maillot, François |
author_facet | Bigot, Adrien Brunault, Paul Lavigne, Christian Feillet, François Odent, Sylvie Kaphan, Elsa Thauvin, Christel Leguy, Vanessa Broué, Pierre Tchan, Michel C. Maillot, François |
author_sort | Bigot, Adrien |
collection | PubMed |
description | Adult onset urea cycle disorders (UCD) may present with psychiatric symptoms, occasionally as the initial presentation. We aimed to describe the characteristics of patients presenting with a psychiatric adult-onset of UCDs, to discuss which signs could suggest this diagnosis in such a situation, and to determine which tests should be conducted. A survey of psychiatric symptoms occurring in teenagers or adults with UCD was conducted in 2010 among clinicians involved in the French society for the study of inborn errors of metabolism (SFEIM). Fourteen patients from 14 to 57 years old were reported. Agitation was reported in 10 cases, perseveration in 5, delirium in 4, and disinhibition in 3 cases. Three patients had pre-existing psychiatric symptoms. All patients had neurological symptoms associated with psychiatric symptoms, such as ataxia or dysmetria, psychomotor slowing, seizures, or hallucinations. Fluctuations of consciousness and coma were reported in 9 cases. Digestive symptoms were reported in 7 cases. 9 patients had a personal history suggestive of UCD. The differential diagnoses most frequently considered were exogenous intoxication, non-convulsive status epilepticus, and meningoencephalitis. Hyperammonemia (180–600 μmol/L) was found in all patients. The outcome was severe: mechanical ventilation was required in 10 patients, 5 patients died, and only 4 patients survived without sequelae. Adult onset UCDs can present with predominant psychiatric symptoms, associated with neurological involvement. These patients, as well as patients presenting with a suspicion of intoxication, must have UCD considered and ammonia measured without delay. |
format | Online Article Text |
id | pubmed-5502717 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-55027172017-07-19 Psychiatric adult-onset of urea cycle disorders: A case-series Bigot, Adrien Brunault, Paul Lavigne, Christian Feillet, François Odent, Sylvie Kaphan, Elsa Thauvin, Christel Leguy, Vanessa Broué, Pierre Tchan, Michel C. Maillot, François Mol Genet Metab Rep Research Paper Adult onset urea cycle disorders (UCD) may present with psychiatric symptoms, occasionally as the initial presentation. We aimed to describe the characteristics of patients presenting with a psychiatric adult-onset of UCDs, to discuss which signs could suggest this diagnosis in such a situation, and to determine which tests should be conducted. A survey of psychiatric symptoms occurring in teenagers or adults with UCD was conducted in 2010 among clinicians involved in the French society for the study of inborn errors of metabolism (SFEIM). Fourteen patients from 14 to 57 years old were reported. Agitation was reported in 10 cases, perseveration in 5, delirium in 4, and disinhibition in 3 cases. Three patients had pre-existing psychiatric symptoms. All patients had neurological symptoms associated with psychiatric symptoms, such as ataxia or dysmetria, psychomotor slowing, seizures, or hallucinations. Fluctuations of consciousness and coma were reported in 9 cases. Digestive symptoms were reported in 7 cases. 9 patients had a personal history suggestive of UCD. The differential diagnoses most frequently considered were exogenous intoxication, non-convulsive status epilepticus, and meningoencephalitis. Hyperammonemia (180–600 μmol/L) was found in all patients. The outcome was severe: mechanical ventilation was required in 10 patients, 5 patients died, and only 4 patients survived without sequelae. Adult onset UCDs can present with predominant psychiatric symptoms, associated with neurological involvement. These patients, as well as patients presenting with a suspicion of intoxication, must have UCD considered and ammonia measured without delay. Elsevier 2017-07-06 /pmc/articles/PMC5502717/ /pubmed/28725569 http://dx.doi.org/10.1016/j.ymgmr.2017.07.001 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Bigot, Adrien Brunault, Paul Lavigne, Christian Feillet, François Odent, Sylvie Kaphan, Elsa Thauvin, Christel Leguy, Vanessa Broué, Pierre Tchan, Michel C. Maillot, François Psychiatric adult-onset of urea cycle disorders: A case-series |
title | Psychiatric adult-onset of urea cycle disorders: A case-series |
title_full | Psychiatric adult-onset of urea cycle disorders: A case-series |
title_fullStr | Psychiatric adult-onset of urea cycle disorders: A case-series |
title_full_unstemmed | Psychiatric adult-onset of urea cycle disorders: A case-series |
title_short | Psychiatric adult-onset of urea cycle disorders: A case-series |
title_sort | psychiatric adult-onset of urea cycle disorders: a case-series |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502717/ https://www.ncbi.nlm.nih.gov/pubmed/28725569 http://dx.doi.org/10.1016/j.ymgmr.2017.07.001 |
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