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(E75.2) Other sphingolipidosis
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59 638 in individuals diagnosis other sphingolipidosis confirmed
10 673 deaths with diagnosis other sphingolipidosis
18% mortality rate associated with the disease other sphingolipidosis
Diagnosis other sphingolipidosis is diagnosed Men are 26.00% more likely than Women
37 571
Men receive the diagnosis other sphingolipidosis
5 833 (15.5 %)Died from this diagnosis.
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22 067
Women receive the diagnosis other sphingolipidosis
4 840 (21.9 %)Died from this diagnosis.
Risk Group for the Disease other sphingolipidosis - Men and Women aged 5-9
In Men diagnosis is most often set at age 0-79
Less common in men the disease occurs at Age 80-95+Less common in women the disease occurs at Age 70-95+
In Women diagnosis is most often set at age 0-69
Disease Features other sphingolipidosis
Absence or low individual and public risk
Other sphingolipidosis - what does this mean
Other sphingolipidosis is a group of inherited metabolic disorders caused by the accumulation of sphingolipids in the body due to a defect in the enzyme responsible for their breakdown. this leads to an impairment of the normal metabolic pathways and can cause a wide range of neurological, skeletal, and cardiovascular problems.
What happens during the disease - other sphingolipidosis
Other sphingolipidosis is a group of rare inherited metabolic disorders caused by genetic defects in the enzymes involved in the metabolism of sphingolipids, which are a type of fat found in the body. these defects lead to the accumulation of sphingolipids in cells and tissues of the body, resulting in a wide range of clinical symptoms including neurological, skeletal, and skin manifestations. the exact pathogenesis of other sphingolipidosis is still unknown, but it is believed to involve the disruption of the normal metabolic pathways of sphingolipids.
Clinical Pattern
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How does a doctor diagnose
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Treatment and Medical Assistance
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30 Days of Hospitalization Required
203 Hours Required for Outpatient Treatment
Other sphingolipidosis - Prevention
Other sphingolipidosis can be prevented by avoiding exposure to toxins, eating a healthy diet rich in vitamins and minerals, exercising regularly, and getting regular medical checkups. additionally, individuals should be aware of their family history and genetic predisposition to these disorders and be aware of the signs and symptoms of sphingolipidosis.