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A rare Hb H disease due to the - -(SEA) and 16.6 kb α-thalassemia-2 deletions.
- Source :
-
Hemoglobin [Hemoglobin] 2012; Vol. 36 (2), pp. 200-4. Date of Electronic Publication: 2012 Feb 29. - Publication Year :
- 2012
-
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.
Details
- Language :
- English
- ISSN :
- 1532-432X
- Volume :
- 36
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Hemoglobin
- Publication Type :
- Academic Journal
- Accession number :
- 22376301
- Full Text :
- https://doi.org/10.3109/03630269.2012.655355