- phenotype,
causes elliptocytosis.
Glycophorin C has the
function of
holding band 4.1 to the cell membrane. It is
thought that
elliptocytosis in glycophorin...
-
sickle cells.
Elliptocytes are
commonly ****ociated with
hereditary elliptocytosis. However, they may also be seen in iron
deficiency anemia, sepsis, malaria...
-
advised as a
therapy and may help to
improve the condition.
Hereditary elliptocytosis is a
group of red
blood cell
membrane disorders characterized by elliptical...
-
hereditary elliptocytosis.
Mutations of the
alphaspectrin gene
causes this disease. HPP can be
considered as a
subset of
hereditary elliptocytosis. Genetic...
- is a
blood disorder that is
similar to, but
distinct from
hereditary elliptocytosis. It is
common in some
communities in
Malaysia and
Papua New Guinea,...
- ****ociated with many disorders, such as
hereditary spherocytosis,
hereditary elliptocytosis,
hereditary stomatocytosis, and
paroxysmal nocturnal hemoglobinuria...
- immune-mediated
hemolysis or
hereditary spherocytosis,
elliptocytosis for iron
deficiency or
hereditary elliptocytosis and
schistocytes for
intravascular hemolysis...
-
result in a
variety of
hereditary red
blood cell disorders,
including elliptocytosis type 2, pyropoikilocytosis, and
spherocytic hemolytic anemia. Spectrin...
- as
enzyme deficiencies or
problems with the red
blood cells (i.e.,
elliptocytosis, spherocytosis, hemolysis, glucose-6-phosphate
dehydrogenase deficiency)...
- primary,
autosomal recessive Midface hypoplasia,
hearing impairment,
elliptocytosis, and
nephrocalcinosis Mitochondrial complex 4 deficiency,
nuclear type...
