Sickle cell retinopathy: A literature review

Detalhes bibliográficos
Autor(a) principal: Ribeiro,Marina Viegas Moura Rezende
Data de Publicação: 2017
Outros Autores: Jucá,João Vitor de Omena, Alves,Anna Luyza Correia dos Santos, Ferreira,Caio Victor Oliveira, Barbosa,Fabiano Timbó, Ribeiro,Êurica Adélia Nogueira
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista da Associação Médica Brasileira (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302017001201100
Resumo: Summary Hemoglobinopathies are a group of hereditary diseases that cause quantitative or qualitative changes in the shape, function or synthesis of hemoglobin. One of the most common is sickle cell anemia, which, due to sickling of erythrocytes, causes vaso-occlusive phenomena. Among the possible ocular manifestations, the most representative is retinopathy, which can lead to blindness if left untreated. Therefore, periodic ophthalmologic monitoring of these patients is important for early diagnosis and adequate therapeutic management, which can be done localy by treating the lesions in the eyes, or systemically.
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spelling Sickle cell retinopathy: A literature reviewretinal diseasesanemiasickle cellreviewhemoglobinopathiesSummary Hemoglobinopathies are a group of hereditary diseases that cause quantitative or qualitative changes in the shape, function or synthesis of hemoglobin. One of the most common is sickle cell anemia, which, due to sickling of erythrocytes, causes vaso-occlusive phenomena. Among the possible ocular manifestations, the most representative is retinopathy, which can lead to blindness if left untreated. Therefore, periodic ophthalmologic monitoring of these patients is important for early diagnosis and adequate therapeutic management, which can be done localy by treating the lesions in the eyes, or systemically.Associação Médica Brasileira2017-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302017001201100Revista da Associação Médica Brasileira v.63 n.12 2017reponame:Revista da Associação Médica Brasileira (Online)instname:Associação Médica Brasileira (AMB)instacron:AMB10.1590/1806-9282.63.12.1100info:eu-repo/semantics/openAccessRibeiro,Marina Viegas Moura RezendeJucá,João Vitor de OmenaAlves,Anna Luyza Correia dos SantosFerreira,Caio Victor OliveiraBarbosa,Fabiano TimbóRibeiro,Êurica Adélia Nogueiraeng2018-02-21T00:00:00Zoai:scielo:S0104-42302017001201100Revistahttps://ramb.amb.org.br/ultimas-edicoes/#https://old.scielo.br/oai/scielo-oai.php||ramb@amb.org.br1806-92820104-4230opendoar:2018-02-21T00:00Revista da Associação Médica Brasileira (Online) - Associação Médica Brasileira (AMB)false
dc.title.none.fl_str_mv Sickle cell retinopathy: A literature review
title Sickle cell retinopathy: A literature review
spellingShingle Sickle cell retinopathy: A literature review
Ribeiro,Marina Viegas Moura Rezende
retinal diseases
anemia
sickle cell
review
hemoglobinopathies
title_short Sickle cell retinopathy: A literature review
title_full Sickle cell retinopathy: A literature review
title_fullStr Sickle cell retinopathy: A literature review
title_full_unstemmed Sickle cell retinopathy: A literature review
title_sort Sickle cell retinopathy: A literature review
author Ribeiro,Marina Viegas Moura Rezende
author_facet Ribeiro,Marina Viegas Moura Rezende
Jucá,João Vitor de Omena
Alves,Anna Luyza Correia dos Santos
Ferreira,Caio Victor Oliveira
Barbosa,Fabiano Timbó
Ribeiro,Êurica Adélia Nogueira
author_role author
author2 Jucá,João Vitor de Omena
Alves,Anna Luyza Correia dos Santos
Ferreira,Caio Victor Oliveira
Barbosa,Fabiano Timbó
Ribeiro,Êurica Adélia Nogueira
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Ribeiro,Marina Viegas Moura Rezende
Jucá,João Vitor de Omena
Alves,Anna Luyza Correia dos Santos
Ferreira,Caio Victor Oliveira
Barbosa,Fabiano Timbó
Ribeiro,Êurica Adélia Nogueira
dc.subject.por.fl_str_mv retinal diseases
anemia
sickle cell
review
hemoglobinopathies
topic retinal diseases
anemia
sickle cell
review
hemoglobinopathies
description Summary Hemoglobinopathies are a group of hereditary diseases that cause quantitative or qualitative changes in the shape, function or synthesis of hemoglobin. One of the most common is sickle cell anemia, which, due to sickling of erythrocytes, causes vaso-occlusive phenomena. Among the possible ocular manifestations, the most representative is retinopathy, which can lead to blindness if left untreated. Therefore, periodic ophthalmologic monitoring of these patients is important for early diagnosis and adequate therapeutic management, which can be done localy by treating the lesions in the eyes, or systemically.
publishDate 2017
dc.date.none.fl_str_mv 2017-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302017001201100
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-42302017001201100
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1806-9282.63.12.1100
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Associação Médica Brasileira
publisher.none.fl_str_mv Associação Médica Brasileira
dc.source.none.fl_str_mv Revista da Associação Médica Brasileira v.63 n.12 2017
reponame:Revista da Associação Médica Brasileira (Online)
instname:Associação Médica Brasileira (AMB)
instacron:AMB
instname_str Associação Médica Brasileira (AMB)
instacron_str AMB
institution AMB
reponame_str Revista da Associação Médica Brasileira (Online)
collection Revista da Associação Médica Brasileira (Online)
repository.name.fl_str_mv Revista da Associação Médica Brasileira (Online) - Associação Médica Brasileira (AMB)
repository.mail.fl_str_mv ||ramb@amb.org.br
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