گزارش یک مورد بیمار Hb-Hamadan در استان هرمزگان

Abstractbackground and objectivesb-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.casethe 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).