A CASE REPORT OF HEMOGLOBIN HAMADAN IN HORMOZGAN PROVINCE

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SOLEIMANI H.; MALEKZADEH K.; SHEKARI M.; PARAN F.; BAZMJOU M.; NAMJOU E.; JAFARI M.

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Journal: THE SCIENTIFIC JOURNAL OF IRANIAN BLOOD TRANSFUSION ORGANIZATION (KHOON) Year:2014 | Volume:11 | Issue:3 Page(s): 252-256

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Title

A CASE REPORT OF HEMOGLOBIN HAMADAN IN HORMOZGAN PROVINCE

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Keywords

BLOOD TRANSFUSIONQ3

PREVALENCEQ3

PREVENTIONQ2

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 couples 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 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).

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APA: Copy

SOLEIMANI, H., MALEKZADEH, K., SHEKARI, M., PARAN, F., BAZMJOU, M., NAMJOU, E., & JAFARI, M.. (2014). A CASE REPORT OF HEMOGLOBIN HAMADAN IN HORMOZGAN PROVINCE. THE SCIENTIFIC JOURNAL OF IRANIAN BLOOD TRANSFUSION ORGANIZATION (KHOON), 11(3), 252-256. SID. https://sid.ir/paper/78695/en

Vancouver: Copy

SOLEIMANI H., MALEKZADEH K., SHEKARI M., PARAN F., BAZMJOU M., NAMJOU E., JAFARI M.. A CASE REPORT OF HEMOGLOBIN HAMADAN IN HORMOZGAN PROVINCE. THE SCIENTIFIC JOURNAL OF IRANIAN BLOOD TRANSFUSION ORGANIZATION (KHOON)[Internet]. 2014;11(3):252-256. Available from: https://sid.ir/paper/78695/en

IEEE: Copy

H. SOLEIMANI, K. MALEKZADEH, M. SHEKARI, F. PARAN, M. BAZMJOU, E. NAMJOU, and M. JAFARI, “A CASE REPORT OF HEMOGLOBIN HAMADAN IN HORMOZGAN PROVINCE,” THE SCIENTIFIC JOURNAL OF IRANIAN BLOOD TRANSFUSION ORGANIZATION (KHOON), vol. 11, no. 3, pp. 252–256, 2014, [Online]. Available: https://sid.ir/paper/78695/en

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