Title, Hemoglobinopatias e talassemias. Author, Paulo César Naoum. Publisher, SARVIER, ISBN, , Length, pages. Download scientific diagram | Distribuição de hemoglobinopatias (talassemias e anemia falciforme). from publication: Análise crítica do programa de triagem. Hemoglobinopatias E Talassemias (Em Portuguese do Brasil): Paulo Cesar Naoum: Books –
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Genetics services for hemoglobinopathies in Latin-America.
Our results addressed us to suggest to the routine laboratories, that is important to accomplish the research of alpha Thalassemia among the Sickle Heoglobinopatias trait, with anemia, to verify the interaction with alpha Thalassemia, supplying to the carriers a important information on its hematological profile, genetic pattern of hemoglobinopathies and the appropriated counseling. Estimation of small percentages of foetal haemoglobin.
The cytological evaluation evidenced the presence of alpha Thalassemia.
For these reasons this work had as its objectives: Abnormal hemoglobins studied and counseling in Brazil. The ovalbumin gene- sequence of putative control regions. Sonati E et al. Blackwell Scientific Publications, O valor de p associado a este caso foi de 0, The high rates of hemoglobin pathologies encountered in the population of pregnant women studied shows the necessity of the implantation of tests for these abnormalities in the pre-natal routine, since in this period the mothers uemoglobinopatias more apt to hemoglobknopatias preoccupied with their own health and that of their babies and, however earlier diagnosed the alterations in the hemoglobins, better and more adequate will be the orientations given the couple.
Hemoglobin types in Brazilian population. Prentice HallNew Jersey, Pagliusi 3 Paulo C. Estimation of small percentages of foetal haemoglobin.
Hemoglobinopatias e talassemias – Paulo César Naoum – Google Books
The Brazilian population, presents genes for abnormal hemoglobins with variable frequencies, which are influenced by the founding racial groups. The control of the hemoglobin pathologies has been possible by means of genetic counseling and early diagnosis. Tipos de hemoglobinas em escolares da cidade de Natal, RN. Rapid electrophoresis and quantiation of hemoglobin on cellulose acetate.
Hemoglobinas AS Alfa talassemia importância diagnóstica
Standartizations of laboratory reagents and methods for detection of haemoglobinopathies. Guidelines for the clinical management of thalassemia.
Genetics and public healt: Phenotype-genotype relationships in mendelian disorders: Sudden death in sickle trait. Appropriated counseling and management requires definitive diagnosis.
Stains for inclusions bodies. How to cite this article. Loader S et al. Bootstrap methods and their applications.
Hemoglobinopathies: a study in pregnancy
A prospective regional trial. For the laboratorial diagnosis the blood samples were submitted to electrophoretic procedures in alkaline and acid pH and cytological evaluation of hemoglobin H. Prenatal screening for hemoglobinopathies. Thalassemia screening in Brazil — results for 20 years. Enviado por Flavio flag Denunciar. The population genetics of the haemoglobinopathies.
Nemoglobinopatias World Health Problem, 1,Washington: Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine. Post-transcriptional modification of globin RNA. The clinical follow-up of the homozygotes and the orientation of the heterozygotes and especially the couples at risk represent a more effective mode of acting to avoid the birth of children who are carriers of a genetic disease, that is frequently lethal.
Entre os companheiros analisados, todos apresentaram hemoglobinas normais.
Alpha globin gene duplications in beta thalassemia patients with intact beta globin gene. Pathogenesis and treatment of sickle cell disease.