A significant proportion of children of African descent with HbSβ 0 thalassaemia are inaccurately diagnosed based on phenotypic analyses alone-Reference-Cited by-同舟云学术

A significant proportion of children of African descent with HbSβ 0 thalassaemia are inaccurately diagnosed based on phenotypic analyses alone

Published:2018-05-24 Issue:1 Volume:185 Page:153-156
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Day Melissa E.¹^ORCID,Rodeghier Mark²,Driggers Jennifer³,Bean Christopher J.³,Volanakis Emmanuel J.¹,DeBaun Michael R.¹

Affiliation:

1. Vanderbilt‐Meharry Center of Excellence in Sickle Cell Disease Vanderbilt University Medical Center Nashville TN USA

2. Rodeghier Consultants Chicago IL USA

3. Division of Blood Disorders National Center on Birth Defects and Developmental Disabilities Centers for Disease Control and Prevention Atlanta GA USA

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.15400

Reference10 articles.

1. Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease

2. Discordance between Self-Report and Genetic Confirmation of Sickle Cell Disease Status in African-American Adults

3. A multicenter randomized controlled trial of intravenous magnesium for sickle cell pain crisis in children

4. The acute chest syndrome in sickle cell disease: incidence and risk factors. The Cooperative Study of Sickle Cell Disease

5. Severe Painful Vaso-Occlusive Crises and Mortality in a Contemporary Adult Sickle Cell Anemia Cohort Study

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