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hemoglobin Zurich Albisrieden

highly unstable alpha chain variant causing alpha(+)-thalassemia with substitution: alpha59(E8)Gly to Arg (alpha2)

Also Known As:

Hb Zurich Albisrieden

Networked: 4 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 Zurich Albisrieden: 4
  - Hemeproteins: 194
    - Globins: 2716
      - Hemoglobins: 37188
        Abnormal Hemoglobins: 120
        hemoglobin Zurich Albisrieden: 4

Experts

1.	Du, Li: 2 articles (07/2021 - 04/2015)
2.	Qin, Danqing: 2 articles (07/2021 - 04/2015)
3.	Wang, Jicheng: 2 articles (07/2021 - 04/2015)
4.	Wu, Jing: 2 articles (07/2021 - 04/2015)
5.	Bao, Xiuqin: 1 article (07/2021)
6.	Ding, Hongke: 1 article (07/2021)
7.	He, Wei: 1 article (07/2021)
8.	Shi, Xiaomei: 1 article (07/2021)
9.	Xiong, Ying: 1 article (07/2021)
10.	Yao, Cuize: 1 article (07/2021)

Related Diseases

1.	Hydrops Fetalis (Fetal Edema) 09/01/2016 - "Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (- -SEA/) Deletion." 09/01/2016 - "Therefore, this was a rare case of Hb Bart's hydrops fetalis associated with Hb Zurich Albisrieden." 07/01/2021 - "Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C)."
2.	Thalassemia 04/01/2015 - "The genotype of fetus is also Hb Zurich Albisrieden with α°-thalassemia. " 04/01/2015 - "Hb Zurich Albisrieden with α°-thalassemia lead to severe anemia. " 09/01/2016 - "Hb Zurich-Albisrieden [HBA2: c.178G > C; α59(E8)Gly→Arg (α2)] is a rare nondeletional α-thalassemia (α-thal) that results from a nucleotide substitution at codon 59 of the α2-globin gene. "
3.	Anemia 04/01/2015 - "Hb Zurich Albisrieden with α°-thalassemia lead to severe anemia. " 07/01/2021 - "Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (HBA2:c.178G>C) and Hb Quong Sze (HBA2:c.377T>C)."
4.	alpha-Thalassemia 01/01/2004 - "A new highly unstable alpha chain variant causing alpha(+)-thalassemia: Hb Zurich Albisrieden [alpha59(E8)Gly-->Arg (alpha2)]." 01/01/2004 - "Hb Zurich Albisrieden [alpha59(E8)Gly-->Arg (alpha2)] is not detected at the protein level and leads to alpha(+)-thalassemia (thal)."

Related Drugs and Biologics

1.	Proteins (Proteins, Gene)
2.	Nucleotides
3.	Codon (Codons)
4.	hemoglobin Quong Sze
5.	hemoglobin Bart's