Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/197975
Type: Artigo de periódico
Title: The Genetics Of Blood Disorders: Hereditary Hemoglobinopathies.
Author: Sonati, Maria de Fátima
Costa, Fernando Ferreira
Abstract: To summarize recently published data on the pathophysiology, diagnosis and treatment of sickle cell diseases and beta-thalassemias, the most relevant hereditary hemoglobinopathies in the global population. Searches were run on the MEDLINE and SCIELO databases, limited to the period from 2003 to May 2008, using the terms hereditary hemoglobinopathies, sickle cell diseases and beta-thalassemia. Two books and two chapters were also included. More than 2,000 articles were identified; those providing the most important information and broadest views were selected. Morbidity and mortality rates from sickle cell diseases and beta-thalassemia are still very high and represent an important challenge. Increased understanding of pathophysiological aspects has lead to significant improvements in treatment and prevention of these diseases.
Subject: Anemia, Sickle Cell
Animals
Disease Models, Animal
Humans
Beta-thalassemia
Rights: aberto
Identifier DOI: doi:10.2223/JPED.1802
Address: http://www.ncbi.nlm.nih.gov/pubmed/18791648
Date Issue: 2008
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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