Clinical phenotypes of three children with sickle cell disease caused by HbS/Sicilian (δβ)⁰ -thalassemia deletion

Am J Hematol. 2022 Apr;97(4):E156-E158. doi: 10.1002/ajh.26470. Epub 2022 Jan 26.

Authors

Banu Aygun¹, Adriana Bello², Alexis A Thompson³, Lance Davis⁴, Yanan Sun⁴, Hong-Yuan Luo⁴, Shuaiying Cui⁴, David H K Chui⁴

Affiliations

¹ Cohen Children's Medical Center of New York, New Hyde Park, New York, USA.
² Centro Médico Docente la Trinidad, Caracas, Venezuela.
³ The Ann and Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
⁴ Boston Medical Center, Boston University School of Medicine, Boston, Massachusetts, USA.

PMID: 35045200
DOI: 10.1002/ajh.26470

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Anemia, Sickle Cell* / complications
Anemia, Sickle Cell* / genetics
Fetal Hemoglobin / genetics
Humans
Phenotype
Thalassemia* / genetics
beta-Thalassemia* / genetics

Substances

Fetal Hemoglobin