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Novel mutation in the mitochondrial transfer RNACys gene in a child

dc.contributor.authorAlmeida, L.S.
dc.contributor.authorMartins, E.
dc.contributor.authorSantorelli, F.M.
dc.contributor.authorVilarinho, L.
dc.date.accessioned2014-04-03T11:37:47Z
dc.date.available2014-04-03T11:37:47Z
dc.date.issued2013-09
dc.description.abstractMitochondrial DNA (mtDNA) disorders are an important group of genetic diseases presenting with a multifacet array of clinical manifestations. Highly energy-dependent tissues such as central nervous system and skeletal and cardiac muscles are commonly involved either as multisystem or as isolated organ disease. Characteristic symptoms include epilepsy, myopathy, deafness and ophthalmoplegia, all associated with point mutations in the mtDNA. Pathogenic mtDNA mutations can be heteroplasmic or homoplasmic. Heteroplasmic mutations are typically associated with mutations in mt-tRNA genes. Mutations in mt-tRNAs genes are responsible for the majority of the presentations of a mitochondrial disease being associated with marked clinical heterogeneity. Although tRNA-encoding genes make up only 9% of the entire mitochondrial genome, over 40% of all point mutations reported in the mtDNA are located in tRNA genes. Here, we present a child with vomiting episodes and migraine in whom we found a novel variant in the mitochondrial tRNACys gene.por
dc.identifier.urihttp://hdl.handle.net/10400.18/2218
dc.language.isoengpor
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpor
dc.subjectDoenças Genéticaspor
dc.subjectDoenças Mitocondriaispor
dc.subjectMitochondrial DNApor
dc.titleNovel mutation in the mitochondrial transfer RNACys gene in a childpor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceBarcelona, Espanhapor
oaire.citation.title12th International Congress of Inborn Errors of Metabolism (ICIEM), 3-6 September 2013por
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor

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