Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (–

Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (– –SEA/) Deletion

Published:2016-09-02 Issue:5 Volume:40 Page:353-355
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Yang Xin¹,Yan Jin-Mei¹,Li Jian¹,Xie Xing-Mei¹,Zhou Jian-Ying¹,Li Yan²,Li Dong-Zhi¹

Affiliation:

1. Prenatal Diagnostic Center, Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China;

2. Guangzhou Cord Blood Bank, Guangzhou Women and Children Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong, People’s Republic of China

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2016.1230067

Reference10 articles.

1. Origa R, Moi P, Galanello R, Cao A. ?Thalassemia. In: Pagon RA, Adam MP, Ardinger HH, et al., Eds. GeneReviews®? National Center for Biotechnology Information (NCBI) Bookshelf (www.ncbi.nlm.nih.gov). Seattle, WA, USA: University of Washington, 1993-2016. (Last updated November 21 2013).

2. Hemoglobin H disease: not necessarily a benign disorder

3. A New Highly Unstable α Chain Variant Causing α+‐Thalassemia: Hb Zurich Albisrieden [α59(E8)Gly→Arg (α2)]

4. The Hb H Disease Genotypes in Southern China

5. Hb adana or α259(E8)Gly→Aspβ2, A severely unstable α1-globin variant, observed in combination with the -(α)20.5 KB α-thal-1 deletion in two Turkish patients

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