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Mitochondrial Carbonic Anhydrase VA Deficiency in Neonatal Hyperammonemic Encephalopathy: Case Report

dc.contributor.authorSequeira, S
dc.date.accessioned2022-09-14T12:00:22Z
dc.date.available2022-09-14T12:00:22Z
dc.date.issued2021
dc.description.abstractHyperammonemia can be a potentially fatal disorder, secondary to several different etiologies, most commonly urea cycle defects and organic acidurias. The deficiency of mitochondrial carbonic anhydrase VA, a recently recognized metabolic disorder, results from abnormalities in the CA5A gene. This gene plays an important role in ureagenesis and gluconeogenesis, resulting in a secondary deficiency of several carboxylases and presenting as neonatal hyperammonemic encephalopathy. We describe the case of an almost 5-year-old child who had neonatal encephalopathy secondary to hyperammonemia wherein carbonic anhydrase VA deficiency was identified in him. His growth and development are normal despite no diet or medication for several years. We report this case as fewer than 20 patients have been described in the literature.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationPort J Pediatr 2021;52:117-21pt_PT
dc.identifier.doidoi.org/10.25754/pjp.2021.20243pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/4244
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSociedade Portuguesa de Pediatriapt_PT
dc.subjectBrain Diseases, Metabolic, Inborn/etiologypt_PT
dc.subjectCarbonic Anhydrases/deficiencypt_PT
dc.subjectCarbonic Anhydrases/ geneticspt_PT
dc.subjectInfant, Newbornpt_PT
dc.subjectHyperammonemia/therapypt_PT
dc.subjectHyperammonemia/etiologypt_PT
dc.subjectCase Reportpt_PT
dc.subjectHDE MTBpt_PT
dc.titleMitochondrial Carbonic Anhydrase VA Deficiency in Neonatal Hyperammonemic Encephalopathy: Case Reportpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage121pt_PT
oaire.citation.startPage117pt_PT
oaire.citation.volume52pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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