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

• Main Authors: Ha Ly Thi Thanh (Author), Huong Le Thi Thanh (Author), Long Hoang Luong (Author), Thinh Huy Tran (Author), Su-Ching Liu (Author), Hai Nam Truong (Author), Thanh Van Ta (Author), The - Hung Bui (Author), Van Khanh Tran (Author)
• Format: Book
• Published: Elsevier, 2018-06-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

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...