hereditary elliptocytosis การใช้

A schematic diagram representing the relationships between cytoskeletal molecules as relevant to hereditary elliptocytosis.
Common hereditary elliptocytosis is the most common form of elliptocytosis, and the form most extensively researched.
Almost all forms of hereditary elliptocytosis are autosomal dominant, and both sexes are therefore at equal risk of having the condition.
Disorders of the proteins in these membranes are associated with many disorders, such as hereditary spherocytosis, hereditary elliptocytosis, hereditary stomatocytosis, and paroxysmal nocturnal hemoglobinuria.
The most important exception to this rule of autosomal dominance is for a subtype of hereditary elliptocytosis called hereditary pyropoikilocytosis ( HPP ), which is autosomal recessive.