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Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)

INTRODUCTION: Neuropsychological symptoms are rare in familial hemiplegic migraine (FHM). There are no reports of psychotic symptoms in FHM type 2 (ATP1A2). We examined a family with a FHM phenotype due to a M731T mutation in ATP1A2. A 10-year follow-up allowed us to observe complex auras, including...

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Detalles Bibliográficos
Autores principales: Barros, José, Mendes, Alexandre, Matos, Ilda, Pereira-Monteiro, José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3444541/
https://www.ncbi.nlm.nih.gov/pubmed/22661290
http://dx.doi.org/10.1007/s10194-012-0462-5
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author Barros, José
Mendes, Alexandre
Matos, Ilda
Pereira-Monteiro, José
author_facet Barros, José
Mendes, Alexandre
Matos, Ilda
Pereira-Monteiro, José
author_sort Barros, José
collection PubMed
description INTRODUCTION: Neuropsychological symptoms are rare in familial hemiplegic migraine (FHM). There are no reports of psychotic symptoms in FHM type 2 (ATP1A2). We examined a family with a FHM phenotype due to a M731T mutation in ATP1A2. A 10-year follow-up allowed us to observe complex auras, including psychotic symptoms in two siblings. CASE REPORT: Male, 48 years old, with an aura that included complex illusions with a feeling of time travelling, coincident with other aura features. The aura was regarded as mystical by the patient. Female, 38 years old, with a complex migraine aura, during which she believed she had the ability to time travel and was being followed by lobbyists who wanted to steal this ability from her. DISCUSSION: FHM type 2 must be included in the list of differential diagnoses of acute psychosis in patients with a previous history of migraine aura.
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spelling pubmed-34445412012-09-24 Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2) Barros, José Mendes, Alexandre Matos, Ilda Pereira-Monteiro, José J Headache Pain Brief Report INTRODUCTION: Neuropsychological symptoms are rare in familial hemiplegic migraine (FHM). There are no reports of psychotic symptoms in FHM type 2 (ATP1A2). We examined a family with a FHM phenotype due to a M731T mutation in ATP1A2. A 10-year follow-up allowed us to observe complex auras, including psychotic symptoms in two siblings. CASE REPORT: Male, 48 years old, with an aura that included complex illusions with a feeling of time travelling, coincident with other aura features. The aura was regarded as mystical by the patient. Female, 38 years old, with a complex migraine aura, during which she believed she had the ability to time travel and was being followed by lobbyists who wanted to steal this ability from her. DISCUSSION: FHM type 2 must be included in the list of differential diagnoses of acute psychosis in patients with a previous history of migraine aura. Springer Milan 2012-06-05 /pmc/articles/PMC3444541/ /pubmed/22661290 http://dx.doi.org/10.1007/s10194-012-0462-5 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Brief Report
Barros, José
Mendes, Alexandre
Matos, Ilda
Pereira-Monteiro, José
Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)
title Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)
title_full Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)
title_fullStr Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)
title_full_unstemmed Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)
title_short Psychotic aura symptoms in familial hemiplegic migraine type 2 (ATP1A2)
title_sort psychotic aura symptoms in familial hemiplegic migraine type 2 (atp1a2)
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3444541/
https://www.ncbi.nlm.nih.gov/pubmed/22661290
http://dx.doi.org/10.1007/s10194-012-0462-5
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