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MRI findings of hypomyelination in adenylosuccinate lyase deficiency

Adenylosuccinate lyase deficiency is a rare genetic disorder with few reported cases in the United States. Magnetic resonance imaging findings in the brain include hypomyelination and low generalized parenchymal volume. Presented here is a case in a 3-month-old male who presented with hypotonia and...

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Autores principales: Kayfan, Samar, Yazdani, Rana M., Castillo, Samantha, Wong, Kevin, Miller, Jeffrey H., Pfeifer, Cory M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260459/
https://www.ncbi.nlm.nih.gov/pubmed/30510607
http://dx.doi.org/10.1016/j.radcr.2018.11.001
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author Kayfan, Samar
Yazdani, Rana M.
Castillo, Samantha
Wong, Kevin
Miller, Jeffrey H.
Pfeifer, Cory M.
author_facet Kayfan, Samar
Yazdani, Rana M.
Castillo, Samantha
Wong, Kevin
Miller, Jeffrey H.
Pfeifer, Cory M.
author_sort Kayfan, Samar
collection PubMed
description Adenylosuccinate lyase deficiency is a rare genetic disorder with few reported cases in the United States. Magnetic resonance imaging findings in the brain include hypomyelination and low generalized parenchymal volume. Presented here is a case in a 3-month-old male who presented with hypotonia and seizures and was subsequently diagnosed with adenylosuccinate lyase deficiency. Given the rarity of this diagnosis, findings demonstrated in this case may prompt ordering physicians to broaden their approach to genetic testing in the setting of hypomyelination. Comparison is also made to more common hypomyelinating leukodystrophies.
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spelling pubmed-62604592018-12-03 MRI findings of hypomyelination in adenylosuccinate lyase deficiency Kayfan, Samar Yazdani, Rana M. Castillo, Samantha Wong, Kevin Miller, Jeffrey H. Pfeifer, Cory M. Radiol Case Rep Neuroradiology Adenylosuccinate lyase deficiency is a rare genetic disorder with few reported cases in the United States. Magnetic resonance imaging findings in the brain include hypomyelination and low generalized parenchymal volume. Presented here is a case in a 3-month-old male who presented with hypotonia and seizures and was subsequently diagnosed with adenylosuccinate lyase deficiency. Given the rarity of this diagnosis, findings demonstrated in this case may prompt ordering physicians to broaden their approach to genetic testing in the setting of hypomyelination. Comparison is also made to more common hypomyelinating leukodystrophies. Elsevier 2018-11-22 /pmc/articles/PMC6260459/ /pubmed/30510607 http://dx.doi.org/10.1016/j.radcr.2018.11.001 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 Neuroradiology
Kayfan, Samar
Yazdani, Rana M.
Castillo, Samantha
Wong, Kevin
Miller, Jeffrey H.
Pfeifer, Cory M.
MRI findings of hypomyelination in adenylosuccinate lyase deficiency
title MRI findings of hypomyelination in adenylosuccinate lyase deficiency
title_full MRI findings of hypomyelination in adenylosuccinate lyase deficiency
title_fullStr MRI findings of hypomyelination in adenylosuccinate lyase deficiency
title_full_unstemmed MRI findings of hypomyelination in adenylosuccinate lyase deficiency
title_short MRI findings of hypomyelination in adenylosuccinate lyase deficiency
title_sort mri findings of hypomyelination in adenylosuccinate lyase deficiency
topic Neuroradiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260459/
https://www.ncbi.nlm.nih.gov/pubmed/30510607
http://dx.doi.org/10.1016/j.radcr.2018.11.001
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