The presence of HbS was reported in Turkey for the first time in the late fifties by Aksoy et al.
This was followed by other reports by the same author revealing the presence of several …

Abstract Background Although G6PD deficiency is the most common genetically determined
blood disorder among Iraqis, its molecular basis has only recently been studied among the …

Abstract Background Glucose-6-Phosphate dehydrogenase (G6PD) is a key enzyme of the
pentose monophosphate pathway, and its deficiency is the most common inherited …

In the present study, we determined the frequency of glucose-6-phosphate dehydrogenase
(G6PD) deficiency in Cyprus using two different procedures in two separate adult population …

BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency, affecting more
than 500 million people worldwide, is one of the most common of inherited disorders. There …

BACKGROUND: The G6PD c. 563 C> T deficient mutation is endemic among Mediterranean
populations but its clinical significance is not well delineated. We set up to estimate the …

Abstract Objective: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most
common inherited cause of neonatal hemolytic anemia and jaundice. We investigated the …

Abstract Glucose-6-phosphate dehydrogenase (G6PD) deficiency considered to be the
commonest inherited enzymopathies disorders worldwide including Iraq. Studies have …

Our objective is to determine the frequency of G6PD Mediterranean mutation (Med mut)
among neonates with high or prolonged jaundice in Dakahlia province, Egypt. Seventy …

Results: The highly diverse ethnic background of the Adana population which probably
results from the high level of immigration into this part of Turkey may be one of the most …