Cystic kidney disease digital illustration

Cystic kidney disease Save


ICD-10 code: Q61

Chapter: Congenital malformations, deformations and chromosomal abnormalities

Cystic Kidney Disease: Causes, Symptoms, and Treatment

Cystic kidney disease refers to a group of inherited disorders that cause fluid-filled sacs, or cysts, to develop in the kidneys. This can lead to kidney damage and eventually kidney failure. Here’s what you need to know about cystic kidney disease:

  1. Causes: Cystic kidney disease is caused by genetic mutations that affect the proteins involved in kidney function. There are two main types of cystic kidney disease: autosomal dominant and autosomal recessive. Autosomal dominant cystic kidney disease is the most common type and is caused by mutations in the PKD1 or PKD2 genes. Autosomal recessive cystic kidney disease is less common and is caused by mutations in the PKHD1 gene.
  2. Symptoms: In the early stages, cystic kidney disease may not cause any symptoms. As the cysts grow and multiply, however, they can cause pain in the back or sides, high blood pressure, frequent urination, and blood in the urine. In some cases, cysts can also develop in other organs, such as the liver, pancreas, or spleen.
  3. Treatment: There is no cure for cystic kidney disease, but treatment can help manage the symptoms and slow the progression of kidney damage. Medications may be prescribed to control high blood pressure or reduce pain. In severe cases, dialysis or kidney transplant may be necessary.

If you have a family history of cystic kidney disease, it’s important to talk to your doctor about screening and genetic testing. Early detection and treatment can help prevent or delay kidney failure.

In conclusion, cystic kidney disease is a genetic disorder that can cause serious kidney damage if left untreated. By understanding the causes and symptoms of this condition, you can take steps to manage your health and prevent complications.

Diagnosis Codes for Cystic kidney disease | Q61

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