Paper Information

Journal:   THE SCIENTIFIC JOURNAL OF IRANIAN BLOOD TRANSFUSION ORGANIZATION (KHOON)   FALL 2014 , Volume 11 , Number 3; Page(s) 252 To 256.
 
Paper: 

A CASE REPORT OF HEMOGLOBIN HAMADAN IN HORMOZGAN PROVINCE

 
Author(s):  SOLEIMANI H., MALEKZADEH K.*, SHEKARI M., PARAN F., BAZMJOU M., NAMJOU E., JAFARI M.
 
* MOLECULAR MEDICINE RESEARCH CENTER, HORMOZGAN UNIVERSITY OF MEDICAL SCIENCES, P.O.BOX: 79197-86848, BANDAR ABBAS, IRAN.
 
Abstract: 

Background and Objectives: ? -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).

 
Keyword(s): BLOOD TRANSFUSION, PREVALENCE, PREVENTION
 
References: 
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