| Literature DB >> 18932068 |
Peyman Eshghi1, Armin Rashidi, Azita Zadeh-Vakili, Ebrahim Miri-Moghadam.
Abstract
In a recent study, we demonstrated that, in the Iranian province of Sistan-Baluchestan (S-B), the IVS-I-5 (G > C) beta-thalassemia (beta-thal) mutation is highly prevalent. In the present article we report the hematological phenotype as measured in 289 carriers of this mutation. We evaluate the use of MCV and MCH parameters as proposed in Iran's national screening guidelines for use in this province. The Hb A(2) cut off of 3.5%, also recommended in the national guidelines, gave 2.7% false negative, as is to be expected due to coexisting elements such as measurement artefacts and delta-thal.Entities:
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Year: 2008 PMID: 18932068 DOI: 10.1080/03630260802341778
Source DB: PubMed Journal: Hemoglobin ISSN: 0363-0269 Impact factor: 0.849