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(Q61.2) Polycystic kidney, autosomal dominant
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508 390 in individuals diagnosis polycystic kidney, autosomal dominant confirmed
16 824 deaths with diagnosis polycystic kidney, autosomal dominant
3% mortality rate associated with the disease polycystic kidney, autosomal dominant
Diagnosis polycystic kidney, autosomal dominant is diagnosed Men are 2.13% more likely than Women
259 602
Men receive the diagnosis polycystic kidney, autosomal dominant
8 565 (3.3 %)Died from this diagnosis.
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248 788
Women receive the diagnosis polycystic kidney, autosomal dominant
8 259 (3.3 %)Died from this diagnosis.
Risk Group for the Disease polycystic kidney, autosomal dominant - Men and Women aged 0
In Men diagnosis is most often set at age 0-95+
in in men, the disease manifests at any agein in women, the disease manifests at any age
In Women diagnosis is most often set at age 0-95+
Disease Features polycystic kidney, autosomal dominant
Absence or low individual and public risk
Polycystic kidney, autosomal dominant - what does this mean
Polycystic kidney disease is an autosomal dominant genetic disorder in which numerous cysts form in the kidneys, leading to enlargement of the kidneys and eventual kidney failure. the cysts are filled with fluid and are caused by a genetic mutation that affects the development and growth of the kidneys.
What happens during the disease - polycystic kidney, autosomal dominant
Polycystic kidney disease (pkd) is an autosomal dominant genetic disorder characterized by the formation of cysts in the kidneys. it is caused by mutations in the pkd1 and pkd2 genes, which are responsible for the production of proteins that regulate the structure of the kidneys. the cysts interfere with the normal functioning of the kidneys, leading to a decrease in the amount of functional tissue and an increase in the amount of fluid. this results in an increased risk of hypertension, kidney failure, and other complications.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- Urinalysis
- Kidney Imaging (Ultrasound, CT scan, MRI)
- Blood tests (Renal Panel, Liver Function Tests)
- Genetic testing
- Renal Biopsy
Treatment and Medical Assistance
Main goal of the treatment: To reduce the symptoms and progression of polycystic kidney disease.
- Regular monitoring of kidney function and blood pressure.
- Reducing salt intake.
- Maintaining a healthy weight.
- Exercising regularly.
- Limiting alcohol consumption.
- Quitting smoking.
- Avoiding certain medications.
- Treating underlying conditions.
- Dialysis or kidney transplant.
12 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Polycystic kidney, autosomal dominant - Prevention
The best way to prevent polycystic kidney, autosomal dominant is to have genetic testing done early in life to determine if a person is carrying the gene. if the gene is present, lifestyle changes such as reducing salt intake, maintaining a healthy weight, and avoiding smoking can help reduce the risk of developing the condition. additionally, regular monitoring of blood pressure and kidney function is important to detect any changes early.