Article
Coinheritance of alpha-thalassemia-1 and hemoglobin E/beta zero-thalassemia: practical implications for neonatal screening and genetic counseling.
The Journal of pediatrics - 1 May 1998
Krishnamurti L, Chui D H, Dallaire M, LeRoy B, Waye J S, Perentesis J P
Abstract excerpt
Hemoglobin E (HbE), alpha-thalassemia, and beta-thalassemia are common among Southeast Asians and often occur in compound heterozygous states that complicate neonatal screening. We describe a kindred with alpha-thalassemia-1, HbE, and beta zero-thalassemia. The proband had HbE/beta zero-thalassemia, with severe anemia and failure to thrive. His father also had HbE/beta zero-thalassemia but had coinherited...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
