ovalocytosis การใช้

There is a ~ 10 % increase in Fy expression in Southeast Asian ovalocytosis erythocytes.
This is reduced in Southeast Asian ovalocytosis a disease of erythrocytes due to a mutation in band 3.
More importantly erythroid AE1 mutations cause 15 25 % of cases of Hereditary spherocytosis ( a disorder associated with progressive red cell membrane loss ), and also cause the hereditary conditions of Hereditary stomatocytosis and Southeast Asian Ovalocytosis
Some of these disorders are known by fanciful and cryptic names like sickle-cell anemia, thalassaemia, glucose-6-phosphate dehydrogenase deficiency, ovalocytosis, elliptocytosis and loss of the Gerbich antigen and the Duffy antigen.