The heritable haemoglobinopathy alpha(+)-thalassaemia is caused by the reduced synthesis of alpha-globin chains that form part of normal adult haemoglobin (Hb). Individuals homozygous for alpha(+)-thalassaemia have microcytosis and an increased erythrocyte count. Alpha(+)-thalassaemia homozygosity confers considerable protection against severe malaria. including severe malarial anaemi... https://www.spidertattooz.com/OPI-GelColor-Magnet-Tool-Mauvnetic-Poles-0-5-oz-p21159/