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(Q61.5) Medullary cystic kidney
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508 390 in individuals diagnosis medullary cystic kidney confirmed
16 824 deaths with diagnosis medullary cystic kidney
3% mortality rate associated with the disease medullary cystic kidney
Diagnosis medullary cystic kidney is diagnosed Men are 2.13% more likely than Women
259 602
Men receive the diagnosis medullary cystic kidney
8 565 (3.3 %)Died from this diagnosis.
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248 788
Women receive the diagnosis medullary cystic kidney
8 259 (3.3 %)Died from this diagnosis.
Risk Group for the Disease medullary cystic kidney - 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 medullary cystic kidney
Absence or low individual and public risk
Medullary cystic kidney - what does this mean
Medullary cystic kidney disease is a genetic disorder caused by mutations in the mckd2 gene, which results in the formation of cysts in the medulla of the kidneys. these cysts can lead to kidney failure and other complications, such as hypertension, proteinuria, and urinary tract infections.
What happens during the disease - medullary cystic kidney
Medullary cystic kidney is an inherited disorder caused by mutations in the mckd2 gene. these mutations lead to the abnormal development of the collecting ducts in the kidneys, resulting in the formation of cysts in the medulla of the kidneys, which can cause progressive kidney damage and eventually lead to kidney failure.
Clinical Pattern
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How does a doctor diagnose
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Treatment and Medical Assistance
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12 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Medullary cystic kidney - Prevention
The best way to prevent medullary cystic kidney disease is to maintain a healthy lifestyle. this includes eating a balanced diet, avoiding smoking and excessive alcohol consumption, exercising regularly, and getting regular check-ups with a healthcare provider. genetic counseling may also be recommended for individuals with a family history of the condition.