A Rare Hb H Hydrops Fetalis Syndrome Caused by the – –SEA Deletion in Combination with the Rare Hb Hirosaki Mutation in a Chinese Patient-Reference-Cited by-同舟云学术

A Rare Hb H Hydrops Fetalis Syndrome Caused by the – –SEA Deletion in Combination with the Rare Hb Hirosaki Mutation in a Chinese Patient

Published:2018-07-04 Issue:4 Volume:42 Page:278-280
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Li Qiang¹,Li Yihong²,Zhong Mei²,Zhang Victor Wei³⁴,Jin Wangjie²,Li Shaoyuan³,Li Liyan²

Affiliation:

1. Department of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong Province, People’s Republic of China;

2. Department of Gynecology and Obstetrics, Technology Center of Prenatal Diagnosis and Genetic Diseases Diagnosis, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong Province, People’s Republic of China;

3. AmCare Genomics Lab, Guangzhou, Guangdong Province, People’s Republic of China;

4. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA

Funder

Guangdong Natural Science Fund for Doctor Scholars

Provincial Science and Technology Plan Project of Guangdong Province

Sino-U.S. Joint Development Defects Transformation Medical Center Construction

Publisher

Informa UK Limited

Subject

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

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2018.1536665

Reference15 articles.

1. Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

2. Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem

3. Hydrops Fetalis Secondary to Bart Hemoglobinopathy

4. Hemoglobin H hydrops fetalis syndrome resulting from the association of the - -SEA deletion and the alphaQuong Szealpha mutation in a Chinese woman

5. Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of α thalassaemia (--MED /αTSaudi α)

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1. Genetic counseling and prenatal decision for hemoglobin H disease caused by the rare α2 codon 30 (-GAG) (HBA2: c.91_93delGAG) mutation and the SEA deletion: Case series study;Taiwanese Journal of Obstetrics and Gynecology;2021-07