Acquired hepatocerebral degeneration: A case report

Acquired hepatocerebral degeneration is an underdiagnosed neurologic syndrome characterized by parkinsonism, ataxia or other movement disorders and by neuropsychiatric and cognitive symptoms. It occurs in patients with chronic liver disease, especially those who develop portosystemic shunting and is...

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Autores principales: Listik, Clarice, Machado-Porto, Gislaine Cristina Lopes, de Oliveira, Maira Okada, Porto, Fábio Henrique de Gobbi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação de Neurologia Cognitiva e do Comportamento 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619109/
https://www.ncbi.nlm.nih.gov/pubmed/29213774
http://dx.doi.org/10.1590/S1980-57642012DN06010010
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author Listik, Clarice
Machado-Porto, Gislaine Cristina Lopes
de Oliveira, Maira Okada
Porto, Fábio Henrique de Gobbi
author_facet Listik, Clarice
Machado-Porto, Gislaine Cristina Lopes
de Oliveira, Maira Okada
Porto, Fábio Henrique de Gobbi
author_sort Listik, Clarice
collection PubMed
description Acquired hepatocerebral degeneration is an underdiagnosed neurologic syndrome characterized by parkinsonism, ataxia or other movement disorders and by neuropsychiatric and cognitive symptoms. It occurs in patients with chronic liver disease, especially those who develop portosystemic shunting and is often unrecognized as a cause of cognitive decline. Recently, its pathogenesis has been associated with manganese accumulation in basal ganglia and some treatments proposed. The aim of this article was to report a case and discuss some discoveries in connection with the disease.
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spelling pubmed-56191092017-12-06 Acquired hepatocerebral degeneration: A case report Listik, Clarice Machado-Porto, Gislaine Cristina Lopes de Oliveira, Maira Okada Porto, Fábio Henrique de Gobbi Dement Neuropsychol Case Report Acquired hepatocerebral degeneration is an underdiagnosed neurologic syndrome characterized by parkinsonism, ataxia or other movement disorders and by neuropsychiatric and cognitive symptoms. It occurs in patients with chronic liver disease, especially those who develop portosystemic shunting and is often unrecognized as a cause of cognitive decline. Recently, its pathogenesis has been associated with manganese accumulation in basal ganglia and some treatments proposed. The aim of this article was to report a case and discuss some discoveries in connection with the disease. Associação de Neurologia Cognitiva e do Comportamento 2012 /pmc/articles/PMC5619109/ /pubmed/29213774 http://dx.doi.org/10.1590/S1980-57642012DN06010010 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Listik, Clarice
Machado-Porto, Gislaine Cristina Lopes
de Oliveira, Maira Okada
Porto, Fábio Henrique de Gobbi
Acquired hepatocerebral degeneration: A case report
title Acquired hepatocerebral degeneration: A case report
title_full Acquired hepatocerebral degeneration: A case report
title_fullStr Acquired hepatocerebral degeneration: A case report
title_full_unstemmed Acquired hepatocerebral degeneration: A case report
title_short Acquired hepatocerebral degeneration: A case report
title_sort acquired hepatocerebral degeneration: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5619109/
https://www.ncbi.nlm.nih.gov/pubmed/29213774
http://dx.doi.org/10.1590/S1980-57642012DN06010010
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AT deoliveiramairaokada acquiredhepatocerebraldegenerationacasereport
AT portofabiohenriquedegobbi acquiredhepatocerebraldegenerationacasereport

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