Brain magnetic resonance imaging (MRI) pattern recognition in Pol III-related leukodystrophies
- PMID: 24105487
- DOI: 10.1177/0883073813503902
Brain magnetic resonance imaging (MRI) pattern recognition in Pol III-related leukodystrophies
Abstract
Pol III-related leukodystrophies are caused by mutations in POLR3A and POLR3B genes and all share peculiar imaging and clinical features. The objectives of this study are (1) to define the neuroradiologic pattern in a cohort of POLR3A and POLR3B subjects and (2) to compare the neuroradiologic pattern of Pol III-related leukodystrophies with other hypomyelinating disorders. The magnetic resonance imaging (MRI) examinations of 13 patients with POLR3A and POLR3B mutations and of 14 patients with other hypomyelinating disorders were analyzed. All the subjects with Pol III-related leukodystrophies presented hypomyelination associated with T2 hypointensity of the thalami and/or the pallida. Twelve subjects (92%) presented T2 hypointensity of the optic radiations. Cerebellar atrophy was observed in most patients (92%). The combination of the analyzed criteria identified patients with Pol III-related leukodystrophies with a sensitivity of 84.6% and a specificity of 92.9%.
Keywords: hypomyelination; leukodystrophy; magnetic resonance imaging.
Similar articles
-
Novel compound heterozygous mutations of POLR3A revealed by whole-exome sequencing in a patient with hypomyelination.Brain Dev. 2014 Apr;36(4):315-21. doi: 10.1016/j.braindev.2013.04.011. Epub 2013 May 18. Brain Dev. 2014. PMID: 23694757
-
Different patterns of cerebellar abnormality and hypomyelination between POLR3A and POLR3B mutations.Brain Dev. 2014 Mar;36(3):259-63. doi: 10.1016/j.braindev.2013.03.006. Epub 2013 May 3. Brain Dev. 2014. PMID: 23643445
-
Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism.J Med Genet. 2013 Mar;50(3):194-7. doi: 10.1136/jmedgenet-2012-101357. Epub 2013 Jan 25. J Med Genet. 2013. PMID: 23355746
-
An Algorithmic Approach to MR Imaging of Hypomyelinating Leukodystrophies.J Magn Reson Imaging. 2025 Apr;61(4):1531-1551. doi: 10.1002/jmri.29558. Epub 2024 Aug 20. J Magn Reson Imaging. 2025. PMID: 39165110 Review.
-
POLR3-related leukodystrophy: How do mutations affecting RNA polymerase III subunits cause hypomyelination?Fac Rev. 2021 Feb 5;10:12. doi: 10.12703/r/10-12. eCollection 2021. Fac Rev. 2021. PMID: 33659930 Free PMC article. Review.
Cited by
-
POLR3A variants in hereditary spastic paraplegia and ataxia.Brain. 2018 Jan 1;141(1):e1. doi: 10.1093/brain/awx290. Brain. 2018. PMID: 29228109 Free PMC article. No abstract available.
-
POLR1C variants dysregulate splicing and cause hypomyelinating leukodystrophy.Neurol Genet. 2020 Oct 13;6(6):e524. doi: 10.1212/NXG.0000000000000524. eCollection 2020 Dec. Neurol Genet. 2020. PMID: 33134519 Free PMC article.
-
GJA1 Variants Cause Spastic Paraplegia Associated with Cerebral Hypomyelination.AJNR Am J Neuroradiol. 2019 May;40(5):788-791. doi: 10.3174/ajnr.A6036. Epub 2019 Apr 25. AJNR Am J Neuroradiol. 2019. PMID: 31023660 Free PMC article.
-
Endocrine Aspects of 4H Leukodystrophy: A Case Report and Review of the Literature.Case Rep Endocrinol. 2015;2015:314594. doi: 10.1155/2015/314594. Epub 2015 May 31. Case Rep Endocrinol. 2015. PMID: 26113998 Free PMC article.
-
Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C.J Clin Endocrinol Metab. 2021 Jan 23;106(2):e660-e674. doi: 10.1210/clinem/dgaa700. J Clin Endocrinol Metab. 2021. PMID: 33005949 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical