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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...

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Autores principales: Robbins, Kyle, Arraj, Patrick, Dengle Sanchez, Lauren, Godiyal, Nikhil, Veltkamp, Daniel L., Pfeifer, Cory M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
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.
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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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