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(N07.6) Hereditary nephropathy, not elsewhere classified : dense deposit disease
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20 599 in individuals diagnosis hereditary nephropathy, not elsewhere classified : dense deposit disease confirmed
4 505 deaths with diagnosis hereditary nephropathy, not elsewhere classified : dense deposit disease
22% mortality rate associated with the disease hereditary nephropathy, not elsewhere classified : dense deposit disease
Diagnosis hereditary nephropathy, not elsewhere classified : dense deposit disease is diagnosed Men are 13.15% more likely than Women
11 654
Men receive the diagnosis hereditary nephropathy, not elsewhere classified : dense deposit disease
1 868 (16.0 %)Died from this diagnosis.
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8 945
Women receive the diagnosis hereditary nephropathy, not elsewhere classified : dense deposit disease
2 637 (29.5 %)Died from this diagnosis.
Risk Group for the Disease hereditary nephropathy, not elsewhere classified : dense deposit disease - Men and Women aged 15-19
In Men diagnosis is most often set at age 0-69, 80-84
Less common in men the disease occurs at Age 70-79, 85-95+Less common in women the disease occurs at Age 0-1, 30-39, 45-54, 80-84, 90-95+
In Women diagnosis is most often set at age 0-29, 40-44, 55-79, 85-89
Disease Features hereditary nephropathy, not elsewhere classified : dense deposit disease
Absence or low individual and public risk
Hereditary nephropathy, not elsewhere classified : dense deposit disease - what does this mean
Hereditary nephropathy, not elsewhere classified: dense deposit disease is a rare genetic disorder caused by mutations in the cfhr5 gene, which results in the abnormal accumulation of proteins in the kidneys leading to chronic kidney disease, proteinuria, and end-stage renal failure.
What happens during the disease - hereditary nephropathy, not elsewhere classified : dense deposit disease
Hereditary nephropathy, not elsewhere classified: dense deposit disease is an inherited disorder caused by the buildup of abnormal proteins in the kidneys. this buildup of proteins causes inflammation, scarring, and eventual kidney failure. the exact cause of this disorder is unknown, but it is believed to be related to a genetic mutation or abnormality that affects the kidneys.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Complete medical history and physical examination
- Urine analysis
- Urinalysis
- Urine protein determination
- Renal biopsy
- Kidney imaging tests (ultrasound, CT scan, MRI)
- Renal function tests (blood urea nitrogen, creatinine, electrolytes)
- Genetic testing
- Renal histology
Treatment and Medical Assistance
Main goal of the treatment: To reduce the risk of kidney failure and slow the progression of the disease.
- Regular monitoring of kidney function and urine tests
- Blood pressure management
- Reduction of dietary sodium and protein intake
- Limiting fluid intake
- Medication to reduce proteinuria
- Monitoring for signs of kidney failure
- Regular dialysis or kidney transplantation if necessary
11 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Hereditary nephropathy, not elsewhere classified : dense deposit disease - Prevention
Prevention of hereditary nephropathy, not elsewhere classified : dense deposit disease can be achieved by genetic counselling and testing for the disease as well as lifestyle modifications such as avoiding smoking, limiting alcohol consumption, and reducing salt intake. early detection and treatment is important in order to prevent the progression of the disease and the development of serious complications.