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A case report of Hemoglobin Hamadan in Hormozgan province.
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- Additional Information
- Abstract:
Background and Objectives β-thalassemia is the most common monogenic autosomal recessive all over the world. Therefore, identifying carriers and performing prenatal testing can prevent the birth of a new patient. Case The young couple resident in Bandar Abbas with their son were referred to the Genetic Laboratory with hematological parameters that indicated minor thalassemia and implicated a symptom of an unknown hemoglobin in the father. Based on the genetic study, the father carried a rare mutation in CD56 (GGC > CGC) leading to Hb-Hamadan. Conclusions In this study seems that Hb-Hamdan has no pathological effect and . This point is very important particularly in prenatal diagnosis (PND). [ABSTRACT FROM AUTHOR]
- Abstract:
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