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Genes, crianças e pediatras: osteodistrofia hereditária de Albright

dc.contributor.authorBandeira, A.
dc.contributor.authorMartins, E.
dc.date.accessioned2012-06-26T10:53:58Z
dc.date.available2012-06-26T10:53:58Z
dc.date.issued2010-09
dc.description.abstractA 11 month-old-year boy presented with moon shaped face, limb shortening, deformity of hands and feets, low stature with weight on percentile 95, without macrocephaly. Analytically he presented with hypocalcaemia, hyperphosphatasemia and high parathormone. The skeleton x-ray did not show bone dysplasia. The typical phenotype led to the diagnosis of Osteodistrophy of Albright.por
dc.identifier.citationNascer e Crescer 2010; 19(3): 180-181por
dc.identifier.issn0872-0754
dc.identifier.urihttp://hdl.handle.net/10400.16/1067
dc.language.isoporpor
dc.peerreviewedyespor
dc.publisherNascer e Crescerpor
dc.subjectOsteodistrophy of Albrightpor
dc.titleGenes, crianças e pediatras: osteodistrofia hereditária de Albrightpor
dc.title.alternativeGenes, children and paediatricians: osteodistrophy of Albrightpor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlacePorto, Portugalpor
oaire.citation.endPage181por
oaire.citation.issue19(3)por
oaire.citation.startPage180por
oaire.citation.titleNascer e Crescerpor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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