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Genes, crianças e pediatras: Doença de Menkes

dc.contributor.authorCorreia, J.
dc.contributor.authorRios, M.
dc.contributor.authorFerreira, P.
dc.contributor.authorMartins, E.
dc.contributor.authorBandeira, A.
dc.date.accessioned2014-02-19T16:20:55Z
dc.date.available2014-02-19T16:20:55Z
dc.date.issued2013-09
dc.description.abstractA male newborn, presenting hipotonia and posterior parietal bossing, developed, in the first 12 hours of life, refusal to feed and hypoglycaemia. A cranial ultrasound, skull X-ray and CT scan revealed an occipital and parietal fracture with an underlying haematoma and extensive extracranial soft-tissue swelling. He was submitted to surgical drainage. After 24 hours: new intracerebral bleeding. At the age of two-months he presented abnormal skin and sparse kinky hair. Serum copper and caeruloplasmin levels were below the normal range. Molecular diagnosis of Menkes disease was made by the identification of a new mutation in ATP7A gene.por
dc.identifier.citationNascer e Crescer 2013; 22(3): 191-192por
dc.identifier.issn0872-0754
dc.identifier.urihttp://hdl.handle.net/10400.16/1574
dc.language.isoporpor
dc.peerreviewedyespor
dc.publisherNascer e Crescerpor
dc.subjectCongenital fracturespor
dc.subjectintracerebral bleedingpor
dc.subjectsparse kinky hairpor
dc.titleGenes, crianças e pediatras: Doença de Menkespor
dc.title.alternativeGenes, children and paediatricians: Menkes diseasepor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlacePorto, Portugalpor
oaire.citation.endPage192por
oaire.citation.startPage191por
oaire.citation.titleNascer e Crescerpor
oaire.citation.volume22(3)por
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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