Prenatal diagnosis of a case with SEA-HPFH deletion thalassemia with whole HBB gene deletion

Prenatal diagnosis of a case with SEA-HPFH deletion thalassemia with whole HBB gene deletion

Objective: The thalassemias is a group of hereditary disorders with impaired production of functional hemoglobin. In this report we described a rare case of compound heterozygous mutation of South-East Asia type hereditary persistence of fetal hemoglobin (SEA-HPFH) and β -thalassemia that allowed pr...

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Bibliographic Details
Main Authors: Ha Ly Thi Thanh, Huong Le Thi Thanh, Long Hoang Luong, Thinh Huy Tran, Su-Ching Liu, Hai Nam Truong, Thanh Van Ta, The - Hung Bui, Van Khanh Tran
Format: Article
Language:English
Published: Elsevier 2018-06-01
Series:Taiwanese Journal of Obstetrics & Gynecology
Subjects:
β-Thalassemia
Deletion
Hereditary persistence of fetal hemoglobinemia (HPFH)
Online Access:http://www.sciencedirect.com/science/article/pii/S1028455918300858

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http://www.sciencedirect.com/science/article/pii/S1028455918300858

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