Rare cause of transfusion‐dependent hemolytic anemia: A case report of HbE/Hb Nottingham and literature review

Author:

Aziz Aisyah1ORCID,Baharin Mohd Farid2,Fauzi Muhammad Yusri1,Abdul Hamid Faidatul Syazlin1,Nadarajaw Thiyagar3,Ahmad Rahimah1,Hashim Hafizah4

Affiliation:

1. Hematology Unit, Cancer Research Centre, Institute for Medical Research (IMR), National Institute of Health (NIH) Ministry of Health Malaysia Shah Alam Selangor Malaysia

2. Immunodeficiency & Immunogenetics Unit, Allergy & Immunology Research Centre, Institute for Medical Research (IMR), National Institute of Health (NIH) Ministry of Health Malaysia Shah Alam Selangor Malaysia

3. Department of Pediatrics Hospital Sultanah Bahiyah (HSB) Alor Setar Kedah Malaysia

4. Department of Pathology Hospital Sultanah Bahiyah (HSB) Alor Setar Kedah Malaysia

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference26 articles.

1. The Hemoglobin E Thalassemias

2. A paradigm shift on beta-thalassaemia treatment: How will we manage this old disease with new therapies?

3. TaherA VichinskyEP MusallamK et al.Guidelines for the management of nontransfusion dependent thalassaemia (NTDT).Thalassaemia International Federation;2013. Accessed September 4 2019.http://www.ncbi.nlm.nih.gov/pubmed/24672826

4. HbVar ID 449. Accessed August 23 2021.https://globin.bx.psu.edu/cgi‐bin/hbvar/query_vars3?mode=output&display_format=page&i=449

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