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hemoglobin Agrinio

proline replaces leucine at position 29(B10) of the alpha-chain

Also Known As:

Hb Agrinio

Networked: 5 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 Agrinio: 5
  - Hemeproteins: 194
    - Globins: 2716
      - Hemoglobins: 37188
        Abnormal Hemoglobins: 120
        hemoglobin Agrinio: 5

Experts

1.	Douna, Varvara: 2 articles (01/2010 - 01/2008)
2.	Kanavakis, Emmanuel: 2 articles (01/2010 - 01/2008)
3.	Papassotiriou, Ioannis: 2 articles (01/2010 - 01/2008)
4.	Stamoulakatou, Alexandra: 2 articles (01/2010 - 01/2008)
5.	Traeger-Synodinos, Joanne: 2 articles (01/2010 - 01/2008)
6.	Fylaktou, Irine: 1 article (01/2010)
7.	Ladis, Vasilis: 1 article (01/2010)
8.	Siahanidou, Tania: 1 article (01/2010)
9.	Metaxotou-Mavrommati, Anna: 1 article (01/2008)

Related Diseases

1.	alpha-Thalassemia 08/08/2023 - "We present a Greek patient harboring a Hb Agrinio variant plus the - -Med alpha deletional allele, having an infrequent severe form of alpha thalassemia, in contrast to the typical alpha thalassemic patient and requiring regular red blood cell (RBC) transfusions and chelation treatment. " 01/01/2008 - "Hb Agrinio is a highly unstable variant, classified as a nondeletional alpha-thalassemia (alpha-thal) mutation, which, to date, has only been described in Greece and Cyprus. "
2.	Hemoglobinopathies 08/08/2023 - "Concomitant Presence of Hb Agrinio and - -Med Deletion in a Greek Male Patient with Hemoglobinopathy H: More Severe Phenotype and Literature Review." 05/01/1998 - "An alpha-thalassemic hemoglobinopathy: homozygosity for the HB Agrinio alpha 2-globin chain variant."
3.	beta-Thalassemia (Cooley's Anemia) 01/01/2010 - "Evaluation of the phenotypic presentation of 12 Hb Agrinio homozygotes or compound heterozygotes, diagnosed in a single center in Greece during a 15-year period, found a wide clinical expression, ranging from thalassemia intermedia (with or without transfusion requirement) to Hb H hydrops fetalis, with some phenotype-to-genotype correlation. "
4.	Hydrops Fetalis (Fetal Edema) 01/01/2010 - "Evaluation of the phenotypic presentation of 12 Hb Agrinio homozygotes or compound heterozygotes, diagnosed in a single center in Greece during a 15-year period, found a wide clinical expression, ranging from thalassemia intermedia (with or without transfusion requirement) to Hb H hydrops fetalis, with some phenotype-to-genotype correlation. "
5.	Thalassemia 01/01/2010 - "Hb Agrinio [α29(B10)Leu→Pro] is a highly unstable variant, classified as a nondeletional α-thalassemia (α-thal) mutation. "

Related Drugs and Biologics

1.	Hemoglobins (Hemoglobin)