A Rare Hb H Disease Due to the – –SEAand 16.6 kb α-Thalassemia-2 Deletions

Autor: Punnee Butthep, Sumalee Jindadamrongwech, Suravee Sroymora, Suporn Chuncharunee
Rok vydání: 2012
Předmět:
Zdroj: Hemoglobin. 36:200-204
ISSN: 1532-432X
0363-0269
Popis: 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.
Databáze: OpenAIRE
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