Chapter title |
Expanding the Clinical and Magnetic Resonance Spectrum of Leukoencephalopathy with Thalamus and Brainstem Involvement and High Lactate (LTBL) in a Patient Harboring a Novel EARS2 Mutation.
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Chapter number | 434 |
Book title |
JIMD Reports, Volume 23
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Published in |
JIMD Reports, April 2015
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DOI | 10.1007/8904_2015_434 |
Pubmed ID | |
Book ISBNs |
978-3-66-247466-2, 978-3-66-247467-9
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Authors |
Biancheri, Roberta, Lamantea, Eleonora, Severino, Mariasavina, Diodato, Daria, Pedemonte, Marina, Cassandrini, Denise, Ploederl, Alexandra, Trucco, Federica, Fiorillo, Chiara, Minetti, Carlo, Santorelli, Filippo M, Zeviani, Massimo, Bruno, Claudio, Roberta Biancheri, Eleonora Lamantea, Mariasavina Severino, Daria Diodato, Marina Pedemonte, Denise Cassandrini, Alexandra Ploederl, Federica Trucco, Chiara Fiorillo, Carlo Minetti, Filippo M. Santorelli, Massimo Zeviani, Claudio Bruno, Santorelli, Filippo M. |
Abstract |
Leukoencephalopathy with thalamus and brainstem involvement and high lactate (LTBL) is a novel mitochondrial disease caused by mutations in EARS2, which encodes the mitochondrial glutamyl-tRNA synthetase (mtGluRS). A distinctive brain MRI pattern is the hallmark of the disease.A 6-year-old boy presented at 3 months with feeding difficulties and muscle hypotonia. Brain MRI, at 8 months, showed hyperintensity of the deep cerebral and cerebellar white matter, thalamus, basal ganglia, brainstem, and thin corpus callosum. From the second year of life onward, the child reported global clinical improvement, parallel to partial resolution of brain MRI pattern. However, the last neuroimaging assessment revealed novel lesions within the left caudate and pallidum nuclei. DNA genomic sequencing analysis identified a novel EARS2 mutation.This case expands the clinical and neuroradiological phenotype of LTBL presenting intermediate clinical manifestations between the severe and milder forms of the disease and previously unreported brain MRI features. |
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