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Parry-Romberg syndrome: findings in advanced magnetic resonance imaging sequences - case report

Parry-Romberg syndrome is a rare disease characterized by progressive hemifacial atrophy associated with other systemic changes, including neurological symptoms. Currently, there are few studies exploring the utilization of advanced magnetic resonance sequences in the investigation of this disease....

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Autores principales: de Paula, Rafael Alfenas, Ribeiro, Bruno Niemeyer de Freitas, Bahia, Paulo Roberto Valle, Ribeiro, Renato Niemeyer de Freitas, de Carvalho, Laís Balbi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Colégio Brasileiro de Radiologia e Diagnóstico por Imagem 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337135/
https://www.ncbi.nlm.nih.gov/pubmed/25741077
http://dx.doi.org/10.1590/0100-3984.2013.1699
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author de Paula, Rafael Alfenas
Ribeiro, Bruno Niemeyer de Freitas
Bahia, Paulo Roberto Valle
Ribeiro, Renato Niemeyer de Freitas
de Carvalho, Laís Balbi
author_facet de Paula, Rafael Alfenas
Ribeiro, Bruno Niemeyer de Freitas
Bahia, Paulo Roberto Valle
Ribeiro, Renato Niemeyer de Freitas
de Carvalho, Laís Balbi
author_sort de Paula, Rafael Alfenas
collection PubMed
description Parry-Romberg syndrome is a rare disease characterized by progressive hemifacial atrophy associated with other systemic changes, including neurological symptoms. Currently, there are few studies exploring the utilization of advanced magnetic resonance sequences in the investigation of this disease. The authors report the case of a 45-year-old patient and describe the findings at structural magnetic resonance imaging and at advanced sequences, correlating them with pathophysiological data.
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spelling pubmed-43371352015-03-04 Parry-Romberg syndrome: findings in advanced magnetic resonance imaging sequences - case report de Paula, Rafael Alfenas Ribeiro, Bruno Niemeyer de Freitas Bahia, Paulo Roberto Valle Ribeiro, Renato Niemeyer de Freitas de Carvalho, Laís Balbi Radiol Bras Case Reports Parry-Romberg syndrome is a rare disease characterized by progressive hemifacial atrophy associated with other systemic changes, including neurological symptoms. Currently, there are few studies exploring the utilization of advanced magnetic resonance sequences in the investigation of this disease. The authors report the case of a 45-year-old patient and describe the findings at structural magnetic resonance imaging and at advanced sequences, correlating them with pathophysiological data. Colégio Brasileiro de Radiologia e Diagnóstico por Imagem 2014 /pmc/articles/PMC4337135/ /pubmed/25741077 http://dx.doi.org/10.1590/0100-3984.2013.1699 Text en © Colégio Brasileiro de Radiologia e Diagnóstico por Imagem http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
de Paula, Rafael Alfenas
Ribeiro, Bruno Niemeyer de Freitas
Bahia, Paulo Roberto Valle
Ribeiro, Renato Niemeyer de Freitas
de Carvalho, Laís Balbi
Parry-Romberg syndrome: findings in advanced magnetic resonance imaging sequences - case report
title Parry-Romberg syndrome: findings in advanced magnetic resonance imaging sequences - case report
title_full Parry-Romberg syndrome: findings in advanced magnetic resonance imaging sequences - case report
title_fullStr Parry-Romberg syndrome: findings in advanced magnetic resonance imaging sequences - case report
title_full_unstemmed Parry-Romberg syndrome: findings in advanced magnetic resonance imaging sequences - case report
title_short Parry-Romberg syndrome: findings in advanced magnetic resonance imaging sequences - case report
title_sort parry-romberg syndrome: findings in advanced magnetic resonance imaging sequences - case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337135/
https://www.ncbi.nlm.nih.gov/pubmed/25741077
http://dx.doi.org/10.1590/0100-3984.2013.1699
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