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Rastreio Neonatal de Hemoglobinopatias numa População Residente em Portugal

dc.contributor.authorPeres, MJ
dc.contributor.authorCarreiro, MH
dc.contributor.authorMachado, MC
dc.contributor.authorSeixas, T
dc.contributor.authorPicanço, I
dc.contributor.authorBatalha, L
dc.contributor.authorLavinha, J
dc.contributor.authorMartins, MC
dc.date.accessioned2012-09-03T14:38:47Z
dc.date.available2012-09-03T14:38:47Z
dc.date.issued1996
dc.description.abstractThe primary objective of newborn screening of hemoglobinopathies is the early identification of infants with sickle cell disease, as they are at increased clinical risk. Other goals include the identification of other types of clinically significant hemoglobinopathies and the detection of heterozygous carriers followed by the screening and counselling of family members. We performed a pilot study for the neonatal screening of hemoglobinopathies in 400 samples of cord blood taken from a maternity in Lisbon. We did not find any newborn with sickle cell disease. Six samples were from sickle cell heterozygotes, the respective families were studied and informed. We looked for the presence of alpha-thalassemia at birth in 100 consecutive samples of cord blood, by the presence of Hb Bart's, abnormal red blood cell indices and alpha-globin genotype. The results show an incidence of 10% of alpha-thalassemia (-alpha) carriers and 4% of triple alpha-globin gene carriers. The authors discuss the feasibility of neonatal screening of hemoglobinopathies in a Portuguese-speaking population consisting of a low prevalence of Hb S trait autoclonous group and a high prevalence immigrant minoritypor
dc.identifier.citationActa Med Port. 1996 Apr-Jun; 9 (4-6): 135-9por
dc.identifier.urihttp://hdl.handle.net/10400.17/633
dc.language.isoporpor
dc.peerreviewedyespor
dc.publisherCentro Editor e Livreiro da Ordem dos Médicospor
dc.subjectHemoglobinopatiapor
dc.subjectRastreio Neonatalpor
dc.subjectPortugalpor
dc.subjectTraço Falciformepor
dc.subjectMAC PED
dc.titleRastreio Neonatal de Hemoglobinopatias numa População Residente em Portugalpor
dc.title.alternativeNeonatal Screening of Hemoglobinopathies in a Population Residing in Portugalpor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage139por
oaire.citation.startPage135por
oaire.citation.titleActa Médica Portuguesapor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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