Delta beta thalassemia, a rare hemoglobin variant: An experience from nodal centre in North Indian state
CONTEXT: Fetal hemoglobin (HbF) reduces to <1% few months after birth. However, it can persist beyond infancy into adult life in rare conditions such as delta-beta (δβ) thalassemia and hereditary persistence of HbF. δβ thalassemia is a relatively rare type of thalassemia due to decrease in both b...
Main Authors: | Promil Jain, Nisha Marwah, Niti Dalal, Richa Pawar, Meenu Gill, Sanjay Kumar |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2022-01-01
|
Series: | Journal of Applied Hematology |
Subjects: | |
Online Access: | http://www.jahjournal.org/article.asp?issn=1658-5127;year=2022;volume=13;issue=1;spage=1;epage=4;aulast=Jain |
Similar Items
-
Varied clinical presentation of compound heterozygous thalassemia with delta beta or hereditary persistence of foetal hemoglobin
by: Sneha Waghela, et al.
Published: (2023-03-01) -
Mutation of CCR5 Delta 32 in Umbilical Cord Blood Samples: Future Potential for HIV-1 Cure
by: Vinayak Virupaksh Kedage, et al.
Published: (2020-05-01) -
Detection of BCL11A, HMIP, and XmnI polymorphisms among anemic pregnant women in hospital Universiti Sains Malaysia
by: Yousef Saeed Mohammad Abu Za'ror, et al.
Published: (2022-01-01) -
Estimated level of plasma micro RNA-210 in beta thalassemia patients and its relation to hemoglobin F level and disease severity
by: Homam M Sharshera, et al.
Published: (2023-01-01) -
Efficacy of ruxolitinib as inducer of fetal hemoglobin in primary erythroid cultures from sickle cell and beta-thalassemia patients
by: Alice Pecoraro, et al.
Published: (2019-04-01)