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(E85.8) Other amyloidosis
More details coming soon
102 222 in individuals diagnosis other amyloidosis confirmed
52 500 deaths with diagnosis other amyloidosis
51% mortality rate associated with the disease other amyloidosis
Diagnosis other amyloidosis is diagnosed Men are 6.07% more likely than Women
54 214
Men receive the diagnosis other amyloidosis
32 453 (59.9 %)Died from this diagnosis.
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48 008
Women receive the diagnosis other amyloidosis
20 047 (41.8 %)Died from this diagnosis.
Risk Group for the Disease other amyloidosis - Men and Women aged 70-74
In Men diagnosis is most often set at age 0-14, 20-94
Less common in men the disease occurs at Age 0-1, 15-19, 95+Less common in women the disease occurs at Age 0-1, 95+
In Women diagnosis is most often set at age 0-94
Disease Features other amyloidosis
Absence or low individual and public risk
Other amyloidosis - what does this mean
Other amyloidosis is a group of diseases caused by the abnormal accumulation of misfolded proteins called amyloid in organs and tissues throughout the body. these proteins are produced by the body's own cells, and can form deposits in the heart, kidneys, liver, intestines, skin, and other organs. these deposits can cause organ failure and other health problems.
What happens during the disease - other amyloidosis
Other amyloidosis is a group of rare diseases caused by the abnormal accumulation of misfolded proteins in organs and tissues. these proteins are known as amyloid and they are produced by the body as a result of a mutation in the gene responsible for producing the proteins. this mutation causes the proteins to form clumps that are resistant to degradation, leading to the accumulation and deposition of amyloid in the organs and tissues. symptoms of other amyloidosis can vary depending on the affected organs, but often include fatigue, weight loss, anemia, and organ failure.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Complete medical history and physical exam
- Blood tests to measure levels of amyloid proteins
- Urine tests to detect amyloid proteins
- Biopsy of affected tissue
- Imaging tests such as X-rays, CT scans, or MRI scans
- Electrocardiogram (ECG) to measure heart activity
- Echocardiogram to measure heart function
- Pulmonary function tests to measure lung capacity
- Bone marrow biopsy to check for abnormal blood cells
Treatment and Medical Assistance
Main goal of the Treatment: To reduce the amount of amyloid protein in the body and to reduce the symptoms of the disease.
- Prescription of medications to reduce the production of amyloid protein.
- Blood transfusions to reduce the amount of amyloid protein.
- Bone marrow transplant to replace the damaged bone marrow cells.
- Plasmapheresis to remove the amyloid protein from the body.
- Surgery to remove the affected organs.
- Physical therapy to improve mobility.
- Counseling to help manage stress and anxiety.
- Nutritional counseling to improve diet.
19 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Other amyloidosis - Prevention
Other amyloidosis can be prevented by avoiding known risk factors such as smoking, alcohol, and certain medications, as well as maintaining a healthy diet and lifestyle. early detection and prompt treatment of the underlying condition can also help reduce the risk of developing amyloidosis.