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Genes, crianças e pediatras

dc.contributor.authorCardoso, Cátia
dc.contributor.authorBandeira, Anabela
dc.contributor.authorMartins, Márcia
dc.contributor.authorMartins, Esmeralda
dc.date.accessioned2021-01-06T16:54:12Z
dc.date.available2021-01-06T16:54:12Z
dc.date.issued2012
dc.description.abstractVACTERL association is characterized for vertebral defects, anal atresia, cardiac defects, tracheo-esophageal fistula, renal anomalies, and limb abnormalities. In this patient we found a also a poor weight gain and microcephaly associated with normochromic and normocytic, anemia, uncontrolled glycemia (hypoglycemia and hyperglycemia) and glycosuria with tubulopathy, nephrotic proteinuria and metabolic acidosis with hyperlactacidemia with led us to suspect and confirm a mitochondrial respiratory chain defect.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationNascer e Crescer vol.21 no.4 Porto dez. 2012pt_PT
dc.identifier.issn0872-0754
dc.identifier.urihttp://hdl.handle.net/10400.26/34596
dc.language.isoporpt_PT
dc.publisherScielo Portugalpt_PT
dc.relation.publisherversionhttp://www.scielo.mec.pt/scielo.php?pid=S0872-07542012000400015&script=sci_arttext&tlng=enpt_PT
dc.subjectAssociação VACTERL doença mitocondrialpt_PT
dc.subjectdoença mitocondrialpt_PT
dc.subjectMadeira Islandpt_PT
dc.subjectRegião Autóoma da Madeirapt_PT
dc.subjectostium secundumpt_PT
dc.subjectecocardiografiapt_PT
dc.subjectmitochondrial respiratory chain defect.pt_PT
dc.subjectvertebral defects and atresiapt_PT
dc.subjectcardiac defectspt_PT
dc.subjecttracheo-esophafeal fistulapt_PT
dc.titleGenes, crianças e pediatraspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage267pt_PT
oaire.citation.issue4pt_PT
oaire.citation.startPage266pt_PT
oaire.citation.volume21pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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