Prevalência de hemoglobinopatias na população adulta brasileira: Pesquisa Nacional de Saúde 2014-2015

Prevalência de hemoglobinopatias na população adulta brasileira: Pesquisa Nacional de Saúde 2014-2015

RESUMO: Objetivo: Descrever a prevalência das hemoglobinopatias da população adulta brasileira, segundo exames laboratoriais da Pesquisa Nacional de Saúde. Métodos: Estudo descritivo realizado com os dados laboratoriais da Pesquisa Nacional de Saúde coletados entre os anos de 2014 e 2015. A pesq...

Full description

Bibliographic Details
Main Authors:	Luiz Gastão Rosenfeld, Nydia Strachman Bacal, Maria Alice Martins Cuder, Alanna Gomes da Silva, Ísis Eloah Machado, Cimar Azereido Pereira, Maria de Fátima Marinho de Souza, Deborah Carvalho Malta
Format:	Article
Language:	English
Published:	Associação Brasileira de Pós-Graduação em Saúde Coletiva
Series:	Revista Brasileira de Epidemiologia
Subjects:	Sickle cell anemia Sickle cell trait beta-Thalassemia Hemoglobin C Fetal hemoglobin Neonatal screening
Online Access:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-790X2019000300411&lng=en&tlng=en

Similar Items

Hemoglobinopatias no Distrito Federal, Brasil
by: J. Tavares-Neto, et al.
Published: (1986-03-01)

Efficacy of ruxolitinib as inducer of fetal hemoglobin in primary erythroid cultures from sickle cell and beta-thalassemia patients
by: Alice Pecoraro, et al.
Published: (2019-04-01)

Perspective: A novel prognostic for sickle cell disease
by: Brian M Mozeleski, et al.
Published: (2018-01-01)

Non-S Sickling Hemoglobin Variants: Historical, Genetic, Diagnostic, and Clinical Perspectives
by: Sagir G. Ahmed, et al.
Published: (2021-05-01)

Clinical and laboratory features of Hemoglobin La Desirade variant in association with sickle cell and alpha thalassemia genes
by: Salam Alkindi, et al.
Published: (2021-01-01)

Evaluation of Signaling Pathways Involved in γ-Globin Gene Induction Using Fetal Hemoglobin Inducer Drugs
by: Fakher Rahim, et al.
Published: (2013-07-01)

Evaluation of Signaling Pathways Involved in γ-Globin Gene Induction Using Fetal Hemoglobin Inducer Drugs
by: Fakher Rahim, et al.
Published: (2013-09-01)

Hemoglobin Disorders in Najran Schools’ Children, KSA
by: Jobran Miree J Al-Qahtani
Published: (2014-08-01)

Prevalência de hemoglobinas anormais em recém-nascidos da cidade de Natal, Rio Grande do Norte, Brasil
by: Maria Cristina Pignataro Emerenciano de Araújo, et al.

Estimation of the prevalence of Hemoglobinopathies in Erbil governorate, Kurdistan region of Iraq
by: Sarkar S Aziz, et al.
Published: (2022-01-01)

Clinical features and outcome of sickle cell anemia in a tertiary center: A retrospective cohort study
by: Abdulrahman Musaad Alhumaid, et al.
Published: (2018-01-01)

Programa comunitário de hemoglobinopatias hereditárias em população estudantil brasileira
by: Mariane B. Compri, et al.

Analysis of sickle hemoglobin
by: A Shrestha, et al.
Published: (2013-10-01)

Hemoglobinopathy SD presenting as Hemoglobinopathy SS
by: Sonia Maria Lissa, et al.
Published: (2017-06-01)

Prevention of hemoglobinopathies in Turkey
by: Mehmet Akif Çürük, et al.
Published: (2013-08-01)

ANEMIA SEL SABIT
by: Gede Agus Suwiryawan, et al.
Published: (2013-09-01)

Clinical and laboratory profile of patients with sickle cell anemia
by: Phelipe Gabriel dos Santos Sant'Ana, et al.

Acute macular infarctions in pediatric patients with hemoglobin SS disease
by: Patrick SY. Lee, et al.
Published: (2023-12-01)

A THE EFFECT OF ALPHA THALASSEMIA, HBF and HBC ON HAEMATOLOGICAL PARAMETERS OF SICKLE CELL DISEASE PATIENTS IN IBADAN, NIGERIA.
by: FASOLA ATINUKE
Published: (2022-01-01)

GBT440 inhibits sickling of sickle cell trait blood under in vitro conditions mimicking strenuous exercise
by: Kobina Dufu, et al.
Published: (2016-09-01)

The curious case of hemoglobin DC disease masquerading as sickle cell anemia
by: Samina Hirani, et al.
Published: (2020-05-01)

Risk factors associated with sickle cell retinopathy: findings from the Cooperative Study of Sickle Cell Disease
by: Mohammed Nawaiseh, et al.
Published: (2022-09-01)

Spectrum of hemoglobinopathies in a tertiary care centre
by: Nisha Sharma, et al.
Published: (2020-05-01)

Associations between red blood cell variants and malaria among children and adults from three areas of Uganda: a prospective cohort study
by: Elijah Kakande, et al.
Published: (2020-01-01)

Association between sickle cell and β-thalassemia genes and hemoglobin concentration and anemia in children and non-pregnant women in Sierra Leone: ancillary analysis of data from Sierra Leone’s 2013 National Micronutrient Survey
by: James P. Wirth, et al.
Published: (2018-01-01)

Sickle cell anemia: hierarchical cluster analysis and clinical profile in a cohort in Brazil
by: Valéria de Freitas Dutra, et al.
Published: (2023-01-01)

IS HEMOGLOBIN E GENE WIDELY SPREAD IN THE STATE OF MADHYA PRADESH IN CENTRAL INDIA? EVIDENCE FROM FIVE TYPICAL FAMILIES
by: R S Balgir
Published: (2014-09-01)

Manifestations of HbSE sickle cell disease: a systematic review
by: Ibrahim Khamees, et al.
Published: (2021-06-01)

Red blood cell exchange in sickle cell disease patient with multiple alloantibodies
by: Geet Aggarwal, et al.
Published: (2020-01-01)

A Mechanism of crystallization process of hemoglobin S
by: Carlos Cabal Mirabal, et al.
Published: (2009-08-01)

Patients with sickle cell disease taking hydroxyurea in the Hemocentro Regional de Montes Claros
by: Fernanda Kelle de Souza Santos, et al.
Published: (2011-01-01)

Prevalence of hemoglobinopathies in premarriage individuals referred to Babolsar, Iran (2006-09)
by: Valizadeh F (MD), et al.
Published: (2012-03-01)

Current challenges in the management of patients with sickle cell disease – A report of the Italian experience
by: Giovanna Russo, et al.
Published: (2019-05-01)

Anesthetic management of a patient with sickle β+ thalassemia
by: Saswata Bharati, et al.
Published: (2011-01-01)

Bobby Jackson's Sore Knee
by: Marshall Anderson
Published: (2007-08-01)

Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients
by: Taher Mahmoud, et al.
Published: (2022-10-01)

Human hemoglobin G-Makassar variant masquerading as sickle cell anemia
by: Ahmad Sabry Mohamad, et al.
Published: (2018-09-01)

Management of Hemoglobin Disorders During the COVID-19 Pandemic
by: Sanjana Fatema Chowdhury, et al.
Published: (2020-06-01)

Traço falciforme: heterozigose para hemoglobina S Sickle cell trait: heterozygous for the hemoglobin S
by: Mitiko Murao, et al.
Published: (2007-09-01)

Utility of paper-based sickle cell test compared to sodium metabisulfite sickling test using hemoglobin electrophoresis as a gold standard at Bugando Medical Center, Mwanza
by: Neema N Mkocha, et al.
Published: (2018-01-01)