Abstract:
:A 7-year old boy presented with a history of recurrent respiratory infections and hypochromic microcytic anemia. Iron profiles were normal thereby prompting genetic analysis of α- and β-globin mutations. The first mutation in a BRE motif of the β-globin gene in the proband, sibling and the mother was identified. The proband and his sibling also inherited common α-globin mutations from the father and mother. In all cases, no serious thalassemia disease was detected.
journal_name
Hemoglobinjournal_title
Hemoglobinauthors
Inati A,Abbas HA,Al-Danaf J,Souaid M,Kahale M,Koussa S,Abou Nasr T,Davis L,Luo HY,Chui DHdoi
10.3109/03630269.2013.772523subject
Has Abstractpub_date
2013-01-01 00:00:00pages
171-5issue
2eissn
0363-0269issn
1532-432Xjournal_volume
37pub_type
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