Cargando…
Leigh syndrome: MRI findings in two children
Leigh syndrome is a progressive neurodegenerative disorder of childhood. The symmetrical necrotic lesions in the basal ganglia and/or brainstem which appear as hyperintense lesions on T2-weighted MRI is characteristic and one of the essential diagnostic criteria. Recognising this MR imaging pattern...
Autores principales: | , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Department of Biomedical Imaging, Faculty of Medicine, University of Malaya, Malaysia
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3097793/ https://www.ncbi.nlm.nih.gov/pubmed/21611066 http://dx.doi.org/10.2349/biij.6.1.e6 |
_version_ | 1782203893313175552 |
---|---|
author | Kartikasalwah, AL LH, Ngu |
author_facet | Kartikasalwah, AL LH, Ngu |
author_sort | Kartikasalwah, AL |
collection | PubMed |
description | Leigh syndrome is a progressive neurodegenerative disorder of childhood. The symmetrical necrotic lesions in the basal ganglia and/or brainstem which appear as hyperintense lesions on T2-weighted MRI is characteristic and one of the essential diagnostic criteria. Recognising this MR imaging pattern in a child with neurological problems should prompt the clinician to investigate for Leigh syndrome. We present here two cases of Leigh syndrome due to different biochemical/genetic defects, and discuss the subtle differences in their MR neuroimaging features. |
format | Text |
id | pubmed-3097793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Department of Biomedical Imaging, Faculty of Medicine, University of Malaya, Malaysia |
record_format | MEDLINE/PubMed |
spelling | pubmed-30977932011-05-24 Leigh syndrome: MRI findings in two children Kartikasalwah, AL LH, Ngu Biomed Imaging Interv J Case Report Leigh syndrome is a progressive neurodegenerative disorder of childhood. The symmetrical necrotic lesions in the basal ganglia and/or brainstem which appear as hyperintense lesions on T2-weighted MRI is characteristic and one of the essential diagnostic criteria. Recognising this MR imaging pattern in a child with neurological problems should prompt the clinician to investigate for Leigh syndrome. We present here two cases of Leigh syndrome due to different biochemical/genetic defects, and discuss the subtle differences in their MR neuroimaging features. Department of Biomedical Imaging, Faculty of Medicine, University of Malaya, Malaysia 2010-01-01 /pmc/articles/PMC3097793/ /pubmed/21611066 http://dx.doi.org/10.2349/biij.6.1.e6 Text en © 2010 Biomedical Imaging and Intervention Journal http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kartikasalwah, AL LH, Ngu Leigh syndrome: MRI findings in two children |
title | Leigh syndrome: MRI findings in two children |
title_full | Leigh syndrome: MRI findings in two children |
title_fullStr | Leigh syndrome: MRI findings in two children |
title_full_unstemmed | Leigh syndrome: MRI findings in two children |
title_short | Leigh syndrome: MRI findings in two children |
title_sort | leigh syndrome: mri findings in two children |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3097793/ https://www.ncbi.nlm.nih.gov/pubmed/21611066 http://dx.doi.org/10.2349/biij.6.1.e6 |
work_keys_str_mv | AT kartikasalwahal leighsyndromemrifindingsintwochildren AT lhngu leighsyndromemrifindingsintwochildren |