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Molybdenum cofactor deficiency: Neuroimaging findings
Molybdenum cofactor deficiency is an extremely rare and fatal metabolic disorder that should be considered in the differential diagnosis of hypoxic-ischemic encephalopathy. Magnetic resonance imaging findings are useful in diagnosis. The short-echo-time magnetic resonance spectrum was characterized...
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/PMC6078902/ https://www.ncbi.nlm.nih.gov/pubmed/30108670 http://dx.doi.org/10.1016/j.radcr.2018.02.025 |
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author | Durmaz, Mehmet Sedat Özbakır, Bora |
author_facet | Durmaz, Mehmet Sedat Özbakır, Bora |
author_sort | Durmaz, Mehmet Sedat |
collection | PubMed |
description | Molybdenum cofactor deficiency is an extremely rare and fatal metabolic disorder that should be considered in the differential diagnosis of hypoxic-ischemic encephalopathy. Magnetic resonance imaging findings are useful in diagnosis. The short-echo-time magnetic resonance spectrum was characterized by a total loss of signal and lipid and lactate peaks. In this case, conventional magnetic resonance imaging and magnetic resonance spectroscopy findings of this extremely rare disease whose pathophysiology was not known were presented. |
format | Online Article Text |
id | pubmed-6078902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-60789022018-08-14 Molybdenum cofactor deficiency: Neuroimaging findings Durmaz, Mehmet Sedat Özbakır, Bora Radiol Case Rep Neuroradiology Molybdenum cofactor deficiency is an extremely rare and fatal metabolic disorder that should be considered in the differential diagnosis of hypoxic-ischemic encephalopathy. Magnetic resonance imaging findings are useful in diagnosis. The short-echo-time magnetic resonance spectrum was characterized by a total loss of signal and lipid and lactate peaks. In this case, conventional magnetic resonance imaging and magnetic resonance spectroscopy findings of this extremely rare disease whose pathophysiology was not known were presented. Elsevier 2018-03-22 /pmc/articles/PMC6078902/ /pubmed/30108670 http://dx.doi.org/10.1016/j.radcr.2018.02.025 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 Durmaz, Mehmet Sedat Özbakır, Bora Molybdenum cofactor deficiency: Neuroimaging findings |
title | Molybdenum cofactor deficiency: Neuroimaging findings |
title_full | Molybdenum cofactor deficiency: Neuroimaging findings |
title_fullStr | Molybdenum cofactor deficiency: Neuroimaging findings |
title_full_unstemmed | Molybdenum cofactor deficiency: Neuroimaging findings |
title_short | Molybdenum cofactor deficiency: Neuroimaging findings |
title_sort | molybdenum cofactor deficiency: neuroimaging findings |
topic | Neuroradiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6078902/ https://www.ncbi.nlm.nih.gov/pubmed/30108670 http://dx.doi.org/10.1016/j.radcr.2018.02.025 |
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