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Neuroimaging Evolution in a Patient With Type 1 Glutaric Aciduria in Treatment Since 7 Months of Age

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dc.creatorCorrea, L. N.spa
dc.creatorBaron, H.spa
dc.date.accessioned2020-07-30T20:58:15Z
dc.date.available2020-07-30T20:58:15Z
dc.date.created2013-07-30spa
dc.description.abstractIntroduction: Glutaric aciduria type 1 is a leukodystrophy. The MRI features can be characteristic and help to establish an early diagnosis. Objectives: A clinical and IRM correlation is performed chronologically after the initiation of the treatment. A direct relationship between imaging and clinical findings has not been described. The IRM evolution and clinical correlation of a patient in current treatment is described since 7 months of age, after presenting his first metabolic crisis. Clinical Course: Macrocephaly at birth, first metabolic crisis at 4 months, dystonia, and previously acquired motor abilities regression. At 7 months, cerebral IRM frontal and opercular hypoplasia with temporal arachnoid cysts, bilateral periventricular leukoencephalopathy, hyperintensity in striated nucleus (t2) were present, hence biochemical confirmation of the diagnosis. Treatment with GAC Med A (formula with free lysine amino acids, low tryptophan), at second year GAC Med B, l carnitine, riboflavin, metabolic rescue treatment with d Ribose 16 months resulted in cerebral parenchyma volume loss, leukoencephalopaty progression, and unchanged basal nucleus. At 3 years, epileptic crisis during a febrile episode was observed. No neuroimaging deterioration was observed. Progressive acquisition of motor development, independent walking, and generalized moderated dystonia. Cognitive and language function are normal as well as nutritional status weight and height. Monitoring has been performed with amino acid and acylcarnitines measurements by mass spectrometry in tandem. Conclusion: After first metabolic crisis, leukodystrophy, and changes in the striated nucleus signal were observed. In the following 2 years, leukodystrophy showed slow progression but the basal nucleus lesions remain equal. Clinically, there is a progressive improvement in the neurodevelopmental motor parameters at 3 years of age, without cognitive deficit or dystonia deteriorationeng
dc.format.mimetypeapplication/pdf
dc.identifier.doihttps://doi.org/10.1177/2326409813511871
dc.identifier.issnISSN: 2326-4098
dc.identifier.issnEISSN: 2326-4594
dc.identifier.urihttps://repository.urosario.edu.co/handle/10336/25614
dc.language.isoengspa
dc.publisherSAGE Publishingspa
dc.relation.citationStartPage33
dc.relation.citationTitleJournal of Inborn Errors of Metabolism and Screening
dc.relation.citationVolumeVol. 1
dc.relation.ispartofJournal of Inborn Errors of Metabolism and Screening, ISSN: 2326-4098, EISSN: 2326-4594, Vol.1 (January, 2013); pp. 33spa
dc.relation.urihttps://journals.sagepub.com/doi/pdf/10.1177/2326409813511871spa
dc.rights.accesRightsinfo:eu-repo/semantics/closedAccess
dc.rights.accesoBloqueado (Texto Referencial)spa
dc.source.instnameinstname:Universidad del Rosariospa
dc.source.reponamereponame:Repositorio Institucional EdocURspa
dc.subject.keywordNeuroimagingspa
dc.subject.keywordType 1 Glutaricspa
dc.subject.keywordTreatmenspa
dc.titleNeuroimaging Evolution in a Patient With Type 1 Glutaric Aciduria in Treatment Since 7 Months of Agespa
dc.typeconferenceObjecteng
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersion
dc.type.spaDocumento de conferenciaspa
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