Literature DB >> 10791557

Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review.

A Ashley-Koch1, Q Yang, R S Olney.   

Abstract

Sickle cell disease is caused by a variant of the beta-globin gene called sickle hemoglobin (Hb S). Inherited autosomal recessively, either two copies of Hb S or one copy of Hb S plus another beta-globin variant (such as Hb C) are required for disease expression. Hb S carriers are protected from malaria infection, and this protection probably led to the high frequency of Hb S in individuals of African and Mediterranean ancestry. Despite this advantage, individuals with sickle cell disease exhibit significant morbidity and mortality. Symptoms include chronic anemia, acute chest syndrome, stroke, splenic and renal dysfunction, pain crises, and susceptibility to bacterial infections. Pediatric mortality is primarily due to bacterial infection and stroke. In adults, specific causes of mortality are more varied, but individuals with more symptomatic disease may exhibit early mortality. Disease expression is variable and is modified by several factors, the most influential being genotype. Other factors include beta-globin cluster haplotypes, alpha-globin gene number, and fetal hemoglobin expression. In recent years, newborn screening, better medical care, parent education, and penicillin prophylaxis have successfully reduced morbidity and mortality due to Hb S.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10791557     DOI: 10.1093/oxfordjournals.aje.a010288

Source DB:  PubMed          Journal:  Am J Epidemiol        ISSN: 0002-9262            Impact factor:   4.897


  117 in total

1.  Genome-wide detection of natural selection in African Americans pre- and post-admixture.

Authors:  Wenfei Jin; Shuhua Xu; Haifeng Wang; Yongguo Yu; Yiping Shen; Bailin Wu; Li Jin
Journal:  Genome Res       Date:  2011-11-29       Impact factor: 9.043

2.  Frequency of sickle cell genotype among the Yorubas in Lagos: implications for the level of awareness and genetic counseling for sickle cell disease in Nigeria.

Authors:  Idowu A Taiwo; Olufemi A Oloyede; Ade O Dosumu
Journal:  J Community Genet       Date:  2011-01-27

3.  An unusual case of a spurious, transfusion-acquired haemoglobin S.

Authors:  Giuseppe Lippi; Mariella Mercadanti; Caleffi Alberta; Massimo Franchini
Journal:  Blood Transfus       Date:  2010-07       Impact factor: 3.443

4.  Photophysical characterization of sickle cell disease hemoglobin by multi-photon microscopy.

Authors:  Genevieve D Vigil; Scott S Howard
Journal:  Biomed Opt Express       Date:  2015-09-24       Impact factor: 3.732

5.  Sickle Cell Disease: Reappraisal of the Role of Foetal Haemoglobin Levels in the Frequency of Vaso-Occlusive Crisis.

Authors:  C Antwi-Boasiako; E Frimpong; G K Ababio; B Dzudzor; I Ekem; B Gyan; N A Sodzi-Tettey; D A Antwi
Journal:  Ghana Med J       Date:  2015-06

6.  Discordance between self-report and genetic confirmation of sickle cell disease status in African-American adults.

Authors:  Christopher J Bean; W Craig Hooper; Dorothy Ellingsen; Michael R DeBaun; Jennifer Sonderman; William J Blot
Journal:  Public Health Genomics       Date:  2014-03-28       Impact factor: 2.000

7.  Emergency department visits made by patients with sickle cell disease: a descriptive study, 1999-2007.

Authors:  Hussain R Yusuf; Hani K Atrash; Scott D Grosse; Christopher S Parker; Althea M Grant
Journal:  Am J Prev Med       Date:  2010-04       Impact factor: 5.043

8.  The prevalence of priapism in children and adolescents with sickle cell disease in Brazil.

Authors:  Paulo Sampaio Furtado; Milena Paiva Costa; Flávia Ribeiro do Prado Valladares; Leandro Oliveira da Silva; Maurício Lordêlo; Isa Lyra; Ubirajara Barroso
Journal:  Int J Hematol       Date:  2012-04-27       Impact factor: 2.490

Review 9.  The role of micronutrients in the response to ambient air pollutants: Potential mechanisms and suggestions for research design.

Authors:  Colette N Miller; Srujana Rayalam
Journal:  J Toxicol Environ Health B Crit Rev       Date:  2017-02-01       Impact factor: 6.393

10.  Autoimmune thyroid disease following alemtuzumab therapy and hematopoietic cell transplantation in pediatric patients with sickle cell disease.

Authors:  Kristen M Williams; Danielle Dietzen; Abeer A Hassoun; Ilene Fennoy; Monica Bhatia
Journal:  Pediatr Blood Cancer       Date:  2014-06-17       Impact factor: 3.167

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.