Hereditary elliptocytosis, also known as ovalocytosis, is an inherited blood disorder in which an abnormally large number of the person's red blood cells...
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of hereditary elliptocytosis. Mutations of the alphaspectrin gene causes this disease. HPP can be considered as a subset of hereditary elliptocytosis. Genetic...
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like sickle cells. Elliptocytes are commonly associated with hereditary elliptocytosis. However, they may also be seen in iron deficiency anemia, sepsis...
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Southeast Asian ovalocytosis (category Hereditary hemolytic anemias)
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...
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There are three major forms of hereditary elliptocytosis: common hereditary elliptocytosis, spherocytic elliptocytosis and southeast Asian ovalocytosis...
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immune-mediated hemolysis or hereditary spherocytosis, elliptocytosis for iron deficiency or hereditary elliptocytosis and schistocytes for intravascular...
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Congenital hemolytic anemia (category Hereditary hemolytic anemias)
be advised as a therapy and may help to improve the condition. Hereditary elliptocytosis is a group of red blood cell membrane disorders characterized...
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aldosteronism Glucose-6-phosphate dehydrogenase deficiency Hepatitis Hereditary elliptocytosis Herpes Heterophoria Human coronaviruses (common cold germs) Hypertension...
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membrane production (as in hereditary spherocytosis and hereditary elliptocytosis). Defects in hemoglobin production (as in thalassemia, sickle-cell disease...
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into the following categories: Membrane conditions Spherocytosis Hereditary elliptocytosis Enzyme conditions Glucose-6-phosphate dehydrogenase deficiency...
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the erythrocytes to be sequestered and destroyed by the spleen. Hereditary elliptocytosis is another defect in membrane skeleton proteins. Abetalipoproteinemia...
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and protein 4.1 are associated with elliptocytosis or spherocytosis and anemia of varying severity. Elliptocytosis is a hematologic disorder characterized...
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Tavares, Simone; Sills, Richard (January 3, 2011). "Pediatric Hereditary Elliptocytosis and Related Disorders". eMedicine. Retrieved 28 March 2011. Yawata...
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Defects of red blood cell membrane production (as in hereditary spherocytosis and hereditary elliptocytosis) Defects in hemoglobin production (as in thalassemia...
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red blood cells) Genetic disorders of RBC membrane Hereditary spherocytosis Hereditary elliptocytosis Congenital dyserythropoietic anemia Genetic disorders...
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relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosis". Blood. 75 (11): 2235–44. doi:10.1182/blood...
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deafness Hereditary elliptocytosis Hereditary fibrinogen Aα-Chain amyloidosis Hereditary fructose intolerance Hereditary hearing disorder Hereditary hearing...
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are associated with many disorders, such as hereditary spherocytosis, hereditary elliptocytosis, hereditary stomatocytosis, and paroxysmal nocturnal hemoglobinuria...
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Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis type 2, pyropoikilocytosis, and spherocytic...
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the concurrence of aldolase A deficiency and dominant (mild) hereditary elliptocytosis, speculatively also relating to ATP depletion. Characterised as...
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in spectrin commonly cause hereditary defects of the erythrocyte, including hereditary elliptocytosis and rarely hereditary spherocytosis. There are three...
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Erythropoietic protoporphyria, caused by mutations in the FECH gene; and hereditary elliptocytosis, caused by mutations in the spectrin gene. ENSG00000105618 GRCh38:...
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unremarkable RBCs, iron deficiency shows anisocytosis, anisochromia and elliptocytosis, and thalassemias demonstrate target cells and coarse basophilic stippling...
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falciparum. Such individuals have a subtype of a condition called hereditary elliptocytosis. The abnormally shaped cells are known as elliptocytes or cameloid...
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(1971). "Erythrocyte glyoxalase II deficiency with coincidental hereditary elliptocytosis". Blood. 36 (6): 797–808. doi:10.1182/blood.V36.6.797.797. PMID 5485124...
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with recessive spherocytic elliptocytosis and recessively transmitted hereditary hemolytic anemia. Hereditary elliptocytosis GRCh38: Ensembl release 89:...
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VIIC; 225410; ADAMTS2 Eiken syndrome; 600002; PTHR1 Elliptocytosis-1; 611804; EPB41 Elliptocytosis-2; 130600; SPTA1 Ellis–van Creveld syndrome; 225500;...
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List of MeSH codes (C16) (section MeSH C16 – congenital, hereditary, and neonatal diseases and abnormalities)
MeSH C16.320.070.150.670 – sickle cell trait MeSH C16.320.070.365 – elliptocytosis, hereditary MeSH C16.320.070.480 – glucosephosphate dehydrogenase deficiency...
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150.150.670 – sickle cell trait MeSH C15.378.071.141.150.365 – elliptocytosis, hereditary MeSH C15.378.071.141.150.480 – glucosephosphate dehydrogenase...
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