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hemoglobin D Iran

abnormality on beta chain; do not confuse with hemoglobin sickle D Iran

Also Known As:

HBB g.1344G>C; Hb D Iran; Hemoglobin D Iran

Networked: 7 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Amino Acids, Peptides, and Proteins: 1
- Proteins: 484843
  - Blood Proteins: 12459
    - Hemoglobins: 37188
      - Abnormal Hemoglobins: 120
        hemoglobin D Iran: 7
  - Hemeproteins: 194
    - Globins: 2716
      - Hemoglobins: 37188
        Abnormal Hemoglobins: 120
        hemoglobin D Iran: 7

Experts

1.	Bhargava, Manorama: 2 articles (06/2017 - 09/2014)
2.	Dass, Jasmita: 2 articles (06/2017 - 09/2014)
3.	Gupta, Aastha: 2 articles (06/2017 - 09/2014)
4.	Saraf, Amrita: 2 articles (06/2017 - 09/2014)
5.	Chen, Gui-Lan: 1 article (12/2017)
6.	Jiang, Fan: 1 article (12/2017)
7.	Qu, Yan-Xia: 1 article (12/2017)
8.	Tang, Fang: 1 article (12/2017)
9.	Tang, Ying: 1 article (12/2017)
10.	Zuo, Lian-Dong: 1 article (12/2017)

Related Diseases

1.	beta-Thalassemia (Cooley's Anemia) 01/01/2001 - "Hb D-Iran has also been described in combination with sickle hemoglobin and beta thalassemia, but never as a homozygous mutation. " 10/01/2014 - "Other variants include Hb Q India, Hb Lepore, Hb J Meerut, Hb D Iran, etc. These variants show heterozygous state along with beta thalassemia. " 01/01/2002 - "Beta thalassemia trait was diagnosed in 21.1%, beta thalassemia major in 0.2%, S-beta thalassemia in 0.37%, Hb D in 0.37%, Hb S trait in 0.32%, Hb E in 0.18%, Hb O-Arab in 0.12%, Hb G-Copenhagen in 0.09%, Hb D-Iran in 0.06%, Hb Lepore in 0.06%, Hb Hasharon in 0.03%. "
2.	Thalassemia 09/01/1973 - "Hemoglobin D Iran alpha A2 beta 22 2-Glu leads to Gln in association with thalassemia." 06/01/2017 - "Twenty-nine cases with Hb D-Iran variant were identified-25 heterozygous, 2 homozygous, 1 compound heterozygous Hb D-Iran/β-thalassemia, and 1 Hb D-Iran/Hb D-Punjab. " 12/01/2017 - "8 kinds of abnormal hemoglobin were detected: Hb E in 102 cases(17 cases with α thalassemia) , Hb Q-Thailand in 20 cases(18 cases with α thalassemia, 2 cases with α and β thalassemia), Hb D-Iran in 4 cases(2 cases with α thalassemia, 1 case with α and β thalassemia), Hb G-Honolulu in 3 cases(1 case with α thalassemia), Hb J-Bangkok in 2 cases(2 cases with α thalassemia), Hb Osu-Christiansborg in 1 case(with α thalassemia), Hb Hasharon in 1 case(with α thalassemia), Hb Koln in 1 case(with α thalassemia). "
3.	Disease Progression 01/01/2001 - "The hematologic values, hemoglobin electrophoresis, peripheral blood smear, and clinical course to date suggest that homozygous Hb D-Iran is a relatively benign condition with mild microcytic anemia, poikilocytosis, and minimal hemolysis."
4.	Hemolysis 01/01/2001 - "The hematologic values, hemoglobin electrophoresis, peripheral blood smear, and clinical course to date suggest that homozygous Hb D-Iran is a relatively benign condition with mild microcytic anemia, poikilocytosis, and minimal hemolysis."
5.	Hemoglobinopathies 09/01/2014 - "Compound heterozygous hemoglobin d-punjab/hemoglobin d-iran: a novel hemoglobinopathy."

Related Drugs and Biologics

1.	Hemoglobins (Hemoglobin)
2.	hemoglobin Lepore
3.	hemoglobin Sealy
4.	hemoglobin D Punjab
5.	Sickle Hemoglobin
6.	hemoglobin Osu-Christiansborg
7.	hemoglobin J Meerut
8.	hemoglobin Q Thailand
9.	hemoglobin Q India
10.	hemoglobin Chinese