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(D58.1) Hereditary elliptocytosis
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140 475 in individuals diagnosis hereditary elliptocytosis confirmed
6 396 deaths with diagnosis hereditary elliptocytosis
5% mortality rate associated with the disease hereditary elliptocytosis
Diagnosis hereditary elliptocytosis is diagnosed Men are 6.51% more likely than Women
74 807
Men receive the diagnosis hereditary elliptocytosis
3 584 (4.8 %)Died from this diagnosis.
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65 668
Women receive the diagnosis hereditary elliptocytosis
2 812 (4.3 %)Died from this diagnosis.
Risk Group for the Disease hereditary elliptocytosis - Men aged 5-9 and Women aged 0-5
In Men diagnosis is most often set at age 0-94
Less common in men the disease occurs at Age 95+Less common in women the disease occurs at Age 95+
In Women diagnosis is most often set at age 0-94
Disease Features hereditary elliptocytosis
Absence or low individual and public risk
Hereditary elliptocytosis - what does this mean
Hereditary elliptocytosis is a genetic disorder caused by a mutation in one of the genes involved in the production of red blood cells. this mutation results in the production of abnormal red blood cells that are shaped like an ellipse rather than the typical round shape. these cells are more prone to breaking apart, leading to anemia and other health problems.
What happens during the disease - hereditary elliptocytosis
Hereditary elliptocytosis is an inherited disorder caused by a genetic mutation that affects the shape of red blood cells. the mutation causes the red blood cells to become elongated or "elliptical" instead of round. this shape change affects the ability of the cells to move through the bloodstream, leading to anemia, fatigue, and jaundice. in some cases, the cells may be so deformed that they are destroyed by the spleen, resulting in further anemia and other complications.
Clinical Pattern
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How does a doctor diagnose
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Treatment and Medical Assistance
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8 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Hereditary elliptocytosis - Prevention
Hereditary elliptocytosis can be prevented by avoiding potential environmental factors that can cause the condition, such as exposure to certain chemicals, alcohol, and drugs. additionally, genetic counseling is recommended for individuals with a family history of the condition.