Correct spelling for the English word "pkd" is [pˌiːkˌe͡ɪdˈiː], [pˌiːkˌeɪdˈiː], [p_ˌiː_k_ˌeɪ_d_ˈiː] (IPA phonetic alphabet).
PKD stands for polycystic kidney disease, which is a genetic disorder characterized by the growth of numerous cysts in the kidneys. It is an inherited condition, meaning it can be passed down through generations within a family. PKD affects both men and women and can manifest itself at any age, although symptoms commonly appear between the ages of 30 and 40.
The cysts that form in the kidneys due to PKD gradually increase in size and number, leading to the enlargement of the kidneys and causing them to lose their ability to function properly. As a result, the kidneys may not efficiently filter waste products from the blood, leading to the accumulation of toxins.
Common symptoms of PKD include high blood pressure, back or side pain, recurrent urinary tract infections, blood in the urine, kidney stones, and frequent urination. In later stages, it can also cause complications such as kidney failure, liver cysts, and heart valve abnormalities.
PKD can be diagnosed through medical imaging techniques such as ultrasound, CT scans, or MRI. Although there is no cure for PKD, treatment focuses on managing symptoms, preventing complications, and preserving kidney function. This may involve medications, lifestyle changes (such as maintaining a healthy diet, regular exercise, and avoiding smoking and excessive alcohol consumption), and, in severe cases, dialysis or kidney transplantation. Genetic testing may also be recommended for family members to determine the risk of inheriting the condition.