Is Estimation of HbA2 Alone Sufficient for Screening Beta Thalassaemia Carriers: A Case in Perspective
Beta thalassaemia is one of the most common inherited haemoglobinopathies, characterised by reduced or absent production of the beta globin chain. In India, the carrier frequency of thalassaemia is estimated to be 3-4%. The prevention of Beta thalassaemia is the best strategy, and this can be achiev...
Main Authors: | Beena Suresh, Umarani Ravichandran, Sujatha Jagadeesh |
---|---|
Format: | Article |
Language: | English |
Published: |
JCDR Research and Publications Private Limited
2023-12-01
|
Series: | Journal of Clinical and Diagnostic Research |
Subjects: | |
Online Access: | https://www.jcdr.net/articles/PDF/18819/67494_CE[Ra1]_F(SL)_QC(KK_RDW_SHU)_PF1(VD_KM_OM)_PFA(VD_KM)_PN(KM).pdf |
Similar Items
-
Genetic tool used to diagnose achromatopsia: first case report from India
by: Kumari Pritti, et al.
Published: (2023-06-01) -
Iron Deficiency Anaemia and Beta Thalassaemia Trait in Anaemic Pregnant Women.
by: Haider H. AL – Shammari
Published: (2010-10-01) -
The Spectrum of the Heterozygous Effect in Biallelic Mendelian Diseases—The Symptomatic Heterozygote Issue
by: Kateryna Kalyta, et al.
Published: (2023-07-01) -
A Carrier Female Manifesting an Unusual X-Linked Retinoschisis Phenotype Associated with the Pathogenic Variant c.266delA, p.(Tyr89LeufsTer37) in <i>RS1</i>, and Skewed X-Inactivation
by: Jennifer Kirkby, et al.
Published: (2023-05-01) -
Heterozygous Pathogenic and Likely Pathogenic Symptomatic HTRA1 Variant Carriers in Cerebral Small Vessel Disease
by: Xu SY, et al.
Published: (2023-03-01)