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Unique neuroradiological findings in propionic acidemia
Propionic acidemia is a rare metabolic disorder that affects the catabolism of branched-chain amino acids and oddchain fatty acids. Propionic acidemia is one of the least common organic acidemias. Presented here are manifestations not previously characterized. The first case is an infant with diffus...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6140419/ https://www.ncbi.nlm.nih.gov/pubmed/30233761 http://dx.doi.org/10.1016/j.radcr.2018.08.011 |
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author | Pfeifer, Cory M. Van Tassel, Dane C. Miller, Jeffrey H. |
author_facet | Pfeifer, Cory M. Van Tassel, Dane C. Miller, Jeffrey H. |
author_sort | Pfeifer, Cory M. |
collection | PubMed |
description | Propionic acidemia is a rare metabolic disorder that affects the catabolism of branched-chain amino acids and oddchain fatty acids. Propionic acidemia is one of the least common organic acidemias. Presented here are manifestations not previously characterized. The first case is an infant with diffuse subcortical diffusion restriction and vermian atrophy. The second case is an adolescent with asymmetric cortical volume loss and contralateral cortical diffusion restriction. These unique brain MRI findings of propionic acidemia may aid the neuroradiologist in guiding genetic testing for occult metabolic disease. |
format | Online Article Text |
id | pubmed-6140419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61404192018-09-19 Unique neuroradiological findings in propionic acidemia Pfeifer, Cory M. Van Tassel, Dane C. Miller, Jeffrey H. Radiol Case Rep Pediatric Propionic acidemia is a rare metabolic disorder that affects the catabolism of branched-chain amino acids and oddchain fatty acids. Propionic acidemia is one of the least common organic acidemias. Presented here are manifestations not previously characterized. The first case is an infant with diffuse subcortical diffusion restriction and vermian atrophy. The second case is an adolescent with asymmetric cortical volume loss and contralateral cortical diffusion restriction. These unique brain MRI findings of propionic acidemia may aid the neuroradiologist in guiding genetic testing for occult metabolic disease. Elsevier 2018-09-14 /pmc/articles/PMC6140419/ /pubmed/30233761 http://dx.doi.org/10.1016/j.radcr.2018.08.011 Text en © 2018 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 | Pediatric Pfeifer, Cory M. Van Tassel, Dane C. Miller, Jeffrey H. Unique neuroradiological findings in propionic acidemia |
title | Unique neuroradiological findings in propionic acidemia |
title_full | Unique neuroradiological findings in propionic acidemia |
title_fullStr | Unique neuroradiological findings in propionic acidemia |
title_full_unstemmed | Unique neuroradiological findings in propionic acidemia |
title_short | Unique neuroradiological findings in propionic acidemia |
title_sort | unique neuroradiological findings in propionic acidemia |
topic | Pediatric |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6140419/ https://www.ncbi.nlm.nih.gov/pubmed/30233761 http://dx.doi.org/10.1016/j.radcr.2018.08.011 |
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