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Genes, crianças e pediatras: Associação VACTERL e doença mitocondrial

dc.contributor.authorCardoso, C.
dc.contributor.authorBandeira, A.
dc.contributor.authorMartins, M.
dc.contributor.authorMartins, E.
dc.date.accessioned2013-05-07T16:42:31Z
dc.date.available2013-05-07T16:42:31Z
dc.date.issued2012-12
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.por
dc.identifier.citationNascer e Crescer 2012; 21(4): 266-267por
dc.identifier.issn0872-0754
dc.identifier.urihttp://hdl.handle.net/10400.16/1425
dc.language.isoporpor
dc.peerreviewedyespor
dc.publisherNascer e Crescerpor
dc.titleGenes, crianças e pediatras: Associação VACTERL e doença mitocondrialpor
dc.title.alternativeGenes, children and paediatricians: VACTERL association and mitochondrial respiratory chain defectpor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlacePorto, Portugalpor
oaire.citation.endPage267por
oaire.citation.startPage266por
oaire.citation.titleNascer e Crescerpor
oaire.citation.volume21(4)por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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