Thalassemia Patients and Friends
Discussion Forums => Thalassemia Minor => Topic started by: Daddy123 on March 05, 2008, 02:43:28 AM
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Dear fellow forumers, I have a question here.
I know that HbA2 >3.5 is a typical diagnosis of Thal carrier / minor. I am just wondering if it is possible for a individual with no Beta Thal trait ( as confirmed by intensive DNA testing ) to have a Hb A2 >3.5 amid slightly eg. 3.5 to 4.
Is there any other conditions that could possibly resulted in a slightly elevated HBA2 apart from being a Beta-Thal carrier ??
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There are other possible explanations for raised Hb A2.
http://www.rcpamanual.edu.au/sections/pathologytest.asp?s=33&i=262
HbA2 is usually raised in the ß thalassaemias, and in unstable haemoglobinopathies where the amino acid substitution is on the ß chain.
Acquired defects of HbA2 also exist. It may also be elevated in thyrotoxicosis (hyperthyroidism) and in megaloblastic anaemias.
Megaloblastic anaemias would be obvious in a blood smear by their size.