Skip navigation
Universidade Federal da Bahia |
Repositório Institucional da UFBA
Use este identificador para citar ou linkar para este item: https://repositorio.ufba.br/handle/ri/5826
Registro completo de metadados
Campo DCValorIdioma
dc.contributor.authorPereira, Maria Betânia-
dc.contributor.authorConceição, Gildásio Carvalho da-
dc.contributor.authorCoelho, Janice C.-
dc.contributor.authorWajner, Moacir-
dc.contributor.authorGiugliani, Roberto-
dc.creatorPereira, Maria Betânia-
dc.creatorConceição, Gildásio Carvalho da-
dc.creatorCoelho, Janice C.-
dc.creatorWajner, Moacir-
dc.creatorGiugliani, Roberto-
dc.date.accessioned2012-05-10T19:31:24Z-
dc.date.available2012-05-10T19:31:24Z-
dc.date.issued1997-
dc.identifier.issn0004-282X-
dc.identifier.urihttp://www.repositorio.ufba.br/ri/handle/ri/5826-
dc.descriptionp.209-212pt_BR
dc.description.abstractThe purpose of this pilot-study was to evaluate the applicability of a screening protocol for the detection of inborn errors of metabolism (IEM) in high-risk patients. The protocol was applied in 65 patients referred to the Medical Genetics Laboratory of the University Hospital Professor Edgard Santos due to the suspicion of na IEM. Eight of these patients (12.3%) displayed an abnormal result in the screening protocol. These patients, along with 22 who displayed normal results in the screening protocol but who presented clinical symptoms or signs suggestive of an IEM not detectable by the tests applied, were selected for a further diagnostic investigation. In 5 of these 30 patients (7.7% of the total sample) it was possible to establish the diagnosis of an specific IEM. The results indicate that the designed screening protocol was sucessfully applied, allowing the detection of affected patients in a frequency comparable to that observed in larger studies performed elsewhere. The continuation of this study and the enlargement of the sample will help to delineate the profile of IEM in northeast of Brazil and will allow the identification of a significative number of patients and families, who could benefit from the therapeutic and preventive measures available for these diseases.pt_BR
dc.language.isoenpt_BR
dc.publisherAssociação Arquivos de Neuro-Psiquiatria Dr. Oswaldo Langept_BR
dc.sourcehttp://dx.doi.org/10.1590/S0004-282X1997000200007pt_BR
dc.subjectMental deficiencypt_BR
dc.subjectInborn errors of metabolismpt_BR
dc.subjectMetabolic disorderspt_BR
dc.subjectAmino acid disorderspt_BR
dc.subjectLysosomal disorderspt_BR
dc.titleDetection of metabolic disorders in high-risk patients: a pilot study in Salvador, Bahiapt_BR
dc.title.alternativeArq Neuropsiquiatrpt_BR
dc.typeArtigo de Periódicopt_BR
dc.description.localpubSão Paulopt_BR
dc.identifier.numberv. 55, n. 2pt_BR
Aparece nas coleções:Artigo Publicado em Periódico (Faculdade de Medicina)

Arquivos associados a este item:
Arquivo Descrição TamanhoFormato 
Pereira, Maria Betânia.pdf406,5 kBAdobe PDFVisualizar/Abrir
Mostrar registro simples do item Visualizar estatísticas


Os itens no repositório estão protegidos por copyright, com todos os direitos reservados, salvo quando é indicado o contrário.