A schematic diagram representing the relationships between cytoskeletal molecules as relevant to hereditary elliptocytosis.
2.
Common hereditary elliptocytosis is the most common form of elliptocytosis, and the form most extensively researched.
3.
Almost all forms of hereditary elliptocytosis are autosomal dominant, and both sexes are therefore at equal risk of having the condition.
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Disorders of the proteins in these membranes are associated with many disorders, such as hereditary spherocytosis, hereditary elliptocytosis, hereditary stomatocytosis, and paroxysmal nocturnal hemoglobinuria.
5.
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.
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These mutations have a common end result; they destabilise the Figure 2-A schematic diagram representing the relationships between cytoskeletal molecules as relevant to hereditary elliptocytosis.
7.
The incidence of hereditary elliptocytosis is hard to determine, as many sufferers of the milder forms of the disorder are asymptomatic and their condition never comes to medical attention.
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However relation to membrane structural stability has been implicated in the concurrence of aldolase A deficiency and dominant ( mild ) hereditary elliptocytosis, speculatively also relating to ATP depletion.
9.
HPP has been associated with a defect of the erythrocyte membrane protein spectrin and with spectrin deficiency . It was characterized in 1975 . It is considered a severe form of hereditary elliptocytosis.
10.
Because it can confer resistance to malaria, some subtypes of hereditary elliptocytosis are significantly more prevalent in regions where malaria is Malayan natives its incidence is 1500-2000 per 10, 000.
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