Haematophysiological Study of Transfusion Dependent Beta-thalassaemia Patients in a Tertiary Care Hospital of Odisha, India
Introduction: The Transfusion Dependent Beta-thalassaemia (TDT) is an autosomal recessive disorder that affects the red blood cells, both in the decreased as well as absence in production of Adult Haemoglobin (HbA) and characterised by severe anaemia, splenomegaly and bone deformities and require li...
Main Authors: | Bhagyalaxmi Das, Bishnu Prasad Dash, Dharma Niranjan Mishra, Rabindra Kumar Jena |
---|---|
Format: | Article |
Language: | English |
Published: |
JCDR Research and Publications Pvt. Ltd.
2023-04-01
|
Series: | National Journal of Laboratory Medicine |
Subjects: | |
Online Access: | https://njlm.net/article_fulltext.aspx?issn=0973-709x&year=2023&month=April&volume=12&issue=2&page=PO11%20-%20PO13&id=2713 |
Similar Items
-
Molecular analysis of haemoglobin E in Southeast Asian populations
by: Wittaya Jomoui, et al.
Published: (2017-11-01) -
Fetal Haemoglobin and β-globin Gene Cluster Haplotypes among Sickle Cell Patients in Chhattisgarh
by: Sanjana Bhagat, et al.
Published: (2013-02-01) -
Red Cell Alloantibodies in Multi - Transfused Patients of Beta Thalassaemia Major
by: Madeeha Rehan
Published: (2015-06-01) -
A Rare Case of Coexistence of Homozygous β-Thalassaemia and Glucose 6 Phosphate Dehydrogenase Deficiency
by: Jitendar Mohan Khunger, et al.
Published: (2020-10-01) -
Challenges in the Diagnosis of Beta-thalassemia Syndrome: The Importance of Molecular Diagnosis
by: Zefarina Zulkafli, et al.
Published: (2022-01-01)