Autosomal Dominant Polycystic Kidney Disease

WHAT YOU NEED TO KNOW:

What is autosomal dominant polycystic kidney disease? Autosomal dominant polycystic kidney disease (ADPKD) is a condition that causes many cysts to grow in your kidneys. ADPKD is most often caused by damaged genes, which are inherited from a parent. The cysts may become large and damage your kidneys. When damage occurs, your kidneys may not work properly, or may stop working completely.
Normal Kidney  Polycystic Kidney

What are the signs and symptoms of ADPKD? You may feel no symptoms during the early stages of ADPKD. Symptoms usually begin between the ages of 30 to 40 years, but may also occur during childhood.

What problems may be caused by ADPKD?

How is ADPKD diagnosed? Tell your healthcare provider if you have family members with ADPKD. He or she may ask what symptoms you feel, when they appeared, and how bad they are. He or she may use any of the following to diagnose ADPKD:

How is ADPKD treated? Currently there is no cure for ADPKD. Treatment may help decrease symptoms and slow the progress of your ADPKD. You may need one or more of the following:

When should I contact my healthcare provider?

When should I seek immediate care or call 911?

CARE AGREEMENT:

You have the right to help plan your care. Learn about your health condition and how it may be treated. Discuss treatment options with your healthcare providers to decide what care you want to receive. You always have the right to refuse treatment. The above information is an educational aid only. It is not intended as medical advice for individual conditions or treatments. Talk to your doctor, nurse or pharmacist before following any medical regimen to see if it is safe and effective for you.

© Copyright Merative 2023 Information is for End User's use only and may not be sold, redistributed or otherwise used for commercial purposes.