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CT and MRI findings in infantile vanishing white matter
Infantile vanishing white matter disease is an uncommon cause of developmental delay and seizures in children. Presented here is a case of vanishing white matter disease diagnosed at 6 months of age. Imaging findings demonstrated widespread white matter abnormalities throughout the supratentorial an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652999/ https://www.ncbi.nlm.nih.gov/pubmed/33204384 http://dx.doi.org/10.1016/j.radcr.2020.10.035 |
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author | Robbins, Kyle Arraj, Patrick Dengle Sanchez, Lauren Godiyal, Nikhil Veltkamp, Daniel L. Pfeifer, Cory M. |
author_facet | Robbins, Kyle Arraj, Patrick Dengle Sanchez, Lauren Godiyal, Nikhil Veltkamp, Daniel L. Pfeifer, Cory M. |
author_sort | Robbins, Kyle |
collection | PubMed |
description | Infantile vanishing white matter disease is an uncommon cause of developmental delay and seizures in children. Presented here is a case of vanishing white matter disease diagnosed at 6 months of age. Imaging findings demonstrated widespread white matter abnormalities throughout the supratentorial and infratentorial brain. The diagnosis of infantile vanishing white matter disease was confirmed via molecular analysis which revealed a rare mutation in the gene responsible for this disorder. |
format | Online Article Text |
id | pubmed-7652999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-76529992020-11-16 CT and MRI findings in infantile vanishing white matter Robbins, Kyle Arraj, Patrick Dengle Sanchez, Lauren Godiyal, Nikhil Veltkamp, Daniel L. Pfeifer, Cory M. Radiol Case Rep Case Report Infantile vanishing white matter disease is an uncommon cause of developmental delay and seizures in children. Presented here is a case of vanishing white matter disease diagnosed at 6 months of age. Imaging findings demonstrated widespread white matter abnormalities throughout the supratentorial and infratentorial brain. The diagnosis of infantile vanishing white matter disease was confirmed via molecular analysis which revealed a rare mutation in the gene responsible for this disorder. Elsevier 2020-11-06 /pmc/articles/PMC7652999/ /pubmed/33204384 http://dx.doi.org/10.1016/j.radcr.2020.10.035 Text en © 2020 The Authors. Published by Elsevier Inc. on behalf of University of Washington. 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 | Case Report Robbins, Kyle Arraj, Patrick Dengle Sanchez, Lauren Godiyal, Nikhil Veltkamp, Daniel L. Pfeifer, Cory M. CT and MRI findings in infantile vanishing white matter |
title | CT and MRI findings in infantile vanishing white matter |
title_full | CT and MRI findings in infantile vanishing white matter |
title_fullStr | CT and MRI findings in infantile vanishing white matter |
title_full_unstemmed | CT and MRI findings in infantile vanishing white matter |
title_short | CT and MRI findings in infantile vanishing white matter |
title_sort | ct and mri findings in infantile vanishing white matter |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7652999/ https://www.ncbi.nlm.nih.gov/pubmed/33204384 http://dx.doi.org/10.1016/j.radcr.2020.10.035 |
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