Publication:
A rare Hb H disease due to the - SEA and 16.6 kb α-thalassemia-2 deletions

Issued Date

2012-04-01

Resource Type

Article

ISSN

1532432X
03630269

DOI

10.3109/03630269.2012.655355

Other identifier(s)

2-s2.0-84858144713

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Hemoglobin. Vol.36, No.2 (2012), 200-204

Suggested Citation

Suravee Sroymora, Sumalee Jindadamrongwech, Punnee Butthep, Suporn Chuncharunee A rare Hb H disease due to the - SEA and 16.6 kb α-thalassemia-2 deletions. Hemoglobin. Vol.36, No.2 (2012), 200-204. doi:10.3109/03630269.2012.655355 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/13764

Research Projects

Organizational Units

Authors

Journal Issue

Thesis

Title

A rare Hb H disease due to the - SEA and 16.6 kb α-thalassemia-2 deletions

Author(s)

Suravee Sroymora
 Sumalee Jindadamrongwech
 Punnee Butthep
 Suporn Chuncharunee

Other Contributor(s)

Faculty of Medicine, Ramathibodi Hospital, Mahidol University
 Mahidol University

Abstract

A large deletional α-thalassemia-2 (α-thal-2) allele was identified in a Thai woman with Hb H disease. The proband has α-thal-1 (SEA type) in conjunction with a 16.6 kb deletion affecting the α2-globin allele. The proband had severe anemia and required a blood transfusion during puerperium. © 2012 Informa Healthcare USA, Inc.

Keyword(s)

Biochemistry, Genetics and Molecular Biology
 Medicine

Availability

URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/13764

Collections

Scopus 2011-2015