Hereditary elliptocytosis, also known as ovalocytosis, is an inherited blood disorder in which an abnormally large number of the person's red blood cells...

of hereditary elliptocytosis. Mutations of the alphaspectrin gene causes this disease. HPP can be considered as a subset of hereditary elliptocytosis. Genetic...

like sickle cells. Elliptocytes are commonly associated with hereditary elliptocytosis. However, they may also be seen in iron deficiency anemia, sepsis...

ovalocytosis 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...

There are three major forms of hereditary elliptocytosis: common hereditary elliptocytosis, spherocytic elliptocytosis and southeast Asian ovalocytosis...

immune-mediated hemolysis or hereditary spherocytosis, elliptocytosis for iron deficiency or hereditary elliptocytosis and schistocytes for intravascular...

be advised as a therapy and may help to improve the condition. Hereditary elliptocytosis is a group of red blood cell membrane disorders characterized...

Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis type 2, pyropoikilocytosis, and spherocytic...

membrane production (as in hereditary spherocytosis and hereditary elliptocytosis). Defects in hemoglobin production (as in thalassemia, sickle-cell disease...

red blood cells) Genetic disorders of RBC membrane Hereditary spherocytosis Hereditary elliptocytosis Congenital dyserythropoietic anemia Genetic disorders...

aldosteronism Glucose-6-phosphate dehydrogenase deficiency Hepatitis Hereditary elliptocytosis Herpes Heterophoria Human coronaviruses (common cold germs) Hypertension...

into the following categories: Membrane conditions Spherocytosis Hereditary elliptocytosis Enzyme conditions Glucose-6-phosphate dehydrogenase deficiency...

the erythrocytes to be sequestered and destroyed by the spleen. Hereditary elliptocytosis is another defect in membrane skeleton proteins. Abetalipoproteinemia...

Defects of red blood cell membrane production (as in hereditary spherocytosis and hereditary elliptocytosis) Defects in hemoglobin production (as in thalassemia...

Tavares, Simone; Sills, Richard (January 3, 2011). "Pediatric Hereditary Elliptocytosis and Related Disorders". eMedicine. Retrieved 28 March 2011. Yawata...

are associated with many disorders, such as hereditary spherocytosis, hereditary elliptocytosis, hereditary stomatocytosis, and paroxysmal nocturnal hemoglobinuria...

and protein 4.1 are associated with elliptocytosis or spherocytosis and anemia of varying severity. Elliptocytosis is a hematologic disorder characterized...

deafness Hereditary elliptocytosis Hereditary fibrinogen Aα-Chain amyloidosis Hereditary fructose intolerance Hereditary hearing disorder Hereditary hearing...

relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis". Blood. 75 (11): 2235–44. doi:10.1182/blood...

in spectrin commonly cause hereditary defects of the erythrocyte, including hereditary elliptocytosis and rarely hereditary spherocytosis. There are three...

the concurrence of aldolase A deficiency and dominant (mild) hereditary elliptocytosis, speculatively also relating to ATP depletion. Characterised as...

falciparum. Such individuals have a subtype of a condition called hereditary elliptocytosis. The abnormally shaped cells are known as elliptocytes or cameloid...

Erythropoietic protoporphyria, caused by mutations in the FECH gene; and hereditary elliptocytosis, caused by mutations in the spectrin gene. ENSG00000105618 GRCh38:...

(1971). "Erythrocyte glyoxalase II deficiency with coincidental hereditary elliptocytosis". Blood. 36 (6): 797–808. doi:10.1182/blood.V36.6.797.797. PMID 5485124...

unremarkable RBCs, iron deficiency shows anisocytosis, anisochromia and elliptocytosis, and thalassemias demonstrate target cells and coarse basophilic stippling...

with recessive spherocytic elliptocytosis and recessively transmitted hereditary hemolytic anemia. Hereditary elliptocytosis GRCh38: Ensembl release 89:...

VIIC; 225410; ADAMTS2 Eiken syndrome; 600002; PTHR1 Elliptocytosis-1; 611804; EPB41 Elliptocytosis-2; 130600; SPTA1 Ellis–van Creveld syndrome; 225500;...

MeSH C16.320.070.150.670 – sickle cell trait MeSH C16.320.070.365 – elliptocytosis, hereditary MeSH C16.320.070.480 – glucosephosphate dehydrogenase deficiency...

150.150.670 – sickle cell trait MeSH C15.378.071.141.150.365 – elliptocytosis, hereditary MeSH C15.378.071.141.150.480 – glucosephosphate dehydrogenase...