hemoglobin D

06/01/2017 - "Haemoglobin electrophoresis showed co-inheritance of haemoglobin D-Punjab and beta thalassemia. "
06/01/2017 - "Here, we present a rare case of co-inheritance of haemoglobin D-Punjab and beta thalassemia in a 19-year-old male of Indian origin. "
06/01/2017 - "Though, haemoglobin D-Punjab is commonly seen, a heterozygous trait with beta thalassemia is a very rare presentation. "
06/01/2017 - "Co-Inheritance of Haemoglobin D-Punjab and Beta Thalassemia - A Rare Variant."
01/01/2012 - "In six patients, the Hb D traits were clinically symptomatic and behaved like those of thalassemia intermedia. "

06/01/2016 - "Hb D: A Not So Rare Hemoglobinopathy."
07/01/1961 - "Hemoglobinopathies in north India--1 hemoglobin D trait and hemoglobin D thelassemia."
04/01/2005 - "Although, compound heterozygous for Hb D/beta-thalassemia has been well described in the literature, our report emphasizes the importance of careful analysis of the electrophoresis results and the usefulness of molecular studies in premarital screening and other screening hemoglobinopathy programs."
09/01/2015 - "These findings corroborated of the National Neonatal Screening Program for diagnosing sickle cell disease and Hb C, Hb D, Hb E and β-thal hemoglobinopathies."
08/01/2020 - "8 kinds of abnormal hemoglobinopathy were detected in 200 cases from 34 800 subjects of child-bearing age, the detection rate was 0.57% in couples of child-bearing age in Chongqing: Among 200 cases of abnormal hemoglobin pathy, Hb E was found in 90 cases (accounting for 45.0%), and Hb D in 25 cases (accounting for 12.5%). "

01/01/2011 - "Hematological studies of the family members showed that thalassemia which caused the mutations and Hb D were in the trans position."
12/01/2022 - "We report on a Pashtun family affected by haemoglobin D-Punjab/β+-thalassemia to increase the awareness of the increasing prevalence of haemoglobinopathies among primary care physicians. "
12/01/2022 - "Diagnosis and clinical relevance of co-inheritance of haemoglobin D-Punjab/β+-thalassemia traits in an immigrant Afghan family."
10/01/2020 - "Is Hemoglobin D Trait Hematologically Silent: Comparison With Healthy Controls and β-thalassemia Carriers."
07/01/2015 - "Serendipity: A Rare Discovery of Haemoglobin D-Iran in An Indian Female During Routine Antenatal Screening for β-Thalassemia."

01/01/2009 - "To study the multi centric origin of this variant which is causing sickle cell disease in association with Hb S [beta6(A3)Glu-->Val, GAG>GTG], we have examined the haplotype of the Hb D allele in different populations. "
07/01/2018 - "Hemoglobin D in a Patient with Sickle Cell Disease (Genotype HbSS)."
01/01/2013 - "Sickle cell hemoglobin D disease (HbSD) is a rare variant of sickle cell disease (SCD). "
07/01/2010 - "Sickle cell hemoglobin D disease is a rare variant of sickle cell disease. "
11/01/2008 - "Hemoglobin D after a red-cell exchange for sickle-cell disease."

01/01/2022 - "The observed Hb D cases were double heterozygous with sickle cell trait (HbSD-Punjab) and manifested symptoms. "
01/01/2003 - "Of 1064 couples aged 14-60 years recruited from the Public Health Laboratory, 49 had beta-thalassaemia trait, 69 had sickle-cell trait, 2 had haemoglobin D trait, 2 had haemoglobin C trait and 1 had high persistent fetal haemoglobin. "
08/01/1998 - "The incidence of haemoglobinopathies within the screened population was 2.62%, and comprised 0.69% beta thalassaemia trait, 1.22% sickle cell trait, 0.43% haemoglobin C trait and 0.26% haemoglobin D trait. "
01/01/1978 - "A case of sickle cell Hb D disease is reported in a young Iranian male, the father of whom carried an AS sickle cell trait and the mother an AD trait. "
01/01/2012 - "β-Thalassemia trait was found in 10.38%, Hb E [β26(B8)Glu→Lys] trait in 4.30%, sickle cell trait in 1.12%, borderline Hb A(2) value 0.73%, low Hb A(2) 0.68% and Hb D trait 0.37%. "