Literature DB >> 25732067

Sickle cell in Latin America and the United States [corrected].

Alexandra Huttle1, Gladys E Maestre2, Rafael Lantigua3, Nancy S Green1.   

Abstract

Latin Americans are an underappreciated population affected by sickle cell disease (SCD). Sickle trait and SCD exist throughout Latin America and U.S. Latino communities. We describe the epidemiology and genetic heterogeneity of SCD among Latin Americans, and fetal hemoglobin expression. National population-based newborn screening for SCD is limited to Brazil, Costa Rica, and the U.S. Available and extrapolated data suggest that over 6,000 annual births and 100,000-150,000 Latin Americans are affected by SCD. This comprehensive review highlights the substantial numbers and population distribution of SCD and sickle trait in Latin America, and where national newborn screening programs for SCD exist.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  Latin America; hemoglobinopathies; sickle cell; sickle trait

Mesh:

Year:  2015        PMID: 25732067     DOI: 10.1002/pbc.25450

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  9 in total

1.  Neonatal screening program for five conditions in Honduras.

Authors:  Michelle Melissa Miralda Buckley; Lindsay Borjas Aguilar; Rosibel Colindres Lainez; Hector Joaquin Alvarado Valenzuela; Fernando Ponce; Débora Gusmão Melo
Journal:  J Community Genet       Date:  2021-01-18

2.  Congolese children with sickle cell trait may exhibit glomerular hyperfiltration: A case control study.

Authors:  Michel Ntetani Aloni; René Makwala Ngiyulu; Célestin Ndosimao Nsibu; Pépé Mfutu Ekulu; Jean Robert Makulo; Jean-Lambert Gini-Ehungu; Nazaire Mangani Nseka; François Bompeka Lepira
Journal:  J Clin Lab Anal       Date:  2017-01-19       Impact factor: 2.352

3.  Quality of Life of Latino and Non-Latino Youth With Sickle Cell Disease as Reported by Parents and Youth.

Authors:  Jennel C Osborne; Nancy S Green; Arlene M Smaldone
Journal:  Hisp Health Care Int       Date:  2020-03-03

Review 4.  Emerging point-of-care technologies for sickle cell disease screening and monitoring.

Authors:  Yunus Alapan; Arwa Fraiwan; Erdem Kucukal; M Noman Hasan; Ryan Ung; Myeongseop Kim; Isaac Odame; Jane A Little; Umut A Gurkan
Journal:  Expert Rev Med Devices       Date:  2016-11-22       Impact factor: 3.166

5.  Food insecurity, housing instability, and dietary quality among children with sickle cell disease: Assessment from a single urban center.

Authors:  Cristina R Fernández; Maureen Licursi; Randi Wolf; Margaret T Lee; Nancy S Green
Journal:  Pediatr Blood Cancer       Date:  2021-11-22       Impact factor: 3.167

6.  High birth prevalence of sickle cell disease in Northwestern Tanzania.

Authors:  Emmanuela E Ambrose; Julie Makani; Neema Chami; Tulla Masoza; Rogatus Kabyemera; Robert N Peck; Erasmus Kamugisha; Alphaxard Manjurano; Neema Kayange; Luke R Smart
Journal:  Pediatr Blood Cancer       Date:  2017-08-02       Impact factor: 3.167

7.  Sickle Cell Trait Induces Oxidative Damage on Plasmodium falciparum Proteome at Erythrocyte Stages.

Authors:  Alber Díaz-Castillo; Neyder Contreras-Puentes; Ciro Alvear-Sedán; Carlos Moneriz-Pretell; Erika Rodríguez-Cavallo; Darío Mendez-Cuadro
Journal:  Int J Mol Sci       Date:  2019-11-16       Impact factor: 5.923

8.  Clinical-Epidemiological Characteristics and Mortality in Patients with Sickle Cell Anemia: A Retrospective Cohort Study of 1980 at 2018.

Authors:  Carolina Mariano Pompeo; Marcos Antonio Ferreira Júnior; Andreia Insabralde de Queiroz Cardoso; Mercy da Costa Souza; Oleci Pereira Frota; Felipe Machado Mota; Maria Lúcia Ivo
Journal:  Int J Gen Med       Date:  2022-02-02

9.  Bibliometric analysis of global sickle cell disease research from 1997 to 2017.

Authors:  Henshaw Uchechi Okoroiwu; Francisco López-Muñoz; F Javier Povedano-Montero
Journal:  Hematol Transfus Cell Ther       Date:  2020-12-28
  9 in total

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