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(E75.5) Other lipid storage disorders
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59 638 in individuals diagnosis other lipid storage disorders confirmed
10 673 deaths with diagnosis other lipid storage disorders
18% mortality rate associated with the disease other lipid storage disorders
Diagnosis other lipid storage disorders is diagnosed Men are 26.00% more likely than Women
37 571
Men receive the diagnosis other lipid storage disorders
5 833 (15.5 %)Died from this diagnosis.
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22 067
Women receive the diagnosis other lipid storage disorders
4 840 (21.9 %)Died from this diagnosis.
Risk Group for the Disease other lipid storage disorders - 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 lipid storage disorders
Absence or low individual and public risk
Other lipid storage disorders - what does this mean
Other lipid storage disorders occur when an individual's body is unable to break down or metabolize fats and lipids properly, leading to an accumulation of lipids in the body's cells and tissues. this accumulation can cause symptoms such as organ dysfunction, neurological problems, and metabolic issues.
What happens during the disease - other lipid storage disorders
Other lipid storage disorders are a group of rare inherited metabolic disorders that are caused by the accumulation of lipids in cells. this accumulation is due to a deficiency in enzymes responsible for breaking down and metabolizing lipids, resulting in the formation of abnormal lipid deposits that can damage organs and tissues. the exact cause of these disorders is unknown, but they are believed to be caused by genetic mutations that affect the production of enzymes responsible for metabolizing lipids.
Clinical Pattern
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How does a doctor diagnose
- Physical exam to assess body fat distribution, skin color, and other physical signs
- Blood tests to measure levels of lipids, including cholesterol and triglycerides
- Genetic testing to identify mutations in genes associated with lipid storage disorders
- Imaging tests, such as ultrasound, to detect any abnormalities in the liver or other organs
- Urine tests to measure levels of fatty acids and other substances
- Liver biopsy to examine liver tissue for signs of lipid accumulation
- Fasting glucose test to check for insulin resistance
- Liver function tests to check for any abnormalities in liver enzymes
Treatment and Medical Assistance
Main goal of the treatment: Reduce the symptoms and improve the quality of life of people suffering from other lipid storage disorders.
- Regular monitoring of the patient's condition.
- Identifying and controlling the risk factors for the disease.
- Nutritional counseling and dietary management.
- Lifestyle modifications such as regular exercise and stress reduction.
- Medication, such as statins, to reduce cholesterol levels.
- Surgery to remove fatty deposits from the body.
- Gene therapy to replace defective genes.
- Stem cell therapy to replace damaged cells.
30 Days of Hospitalization Required
203 Hours Required for Outpatient Treatment
Other lipid storage disorders - Prevention
The best way to prevent other lipid storage disorders is to maintain a healthy diet and lifestyle. eating a balanced diet low in saturated fat and cholesterol, exercising regularly, and avoiding smoking and excessive alcohol consumption can help reduce the risk of developing these disorders. additionally, it is important to follow up with your healthcare provider regularly for recommended screenings and tests.