Polycystic kidney disease (PKD) is an inherited genetic disorder in which numerous fluid-filled cysts develop in the kidneys. As cysts grow and multiply, the kidneys may become enlarged, and their ability to filter blood can gradually decline. PKD can also affect organs outside the kidneys, particularly the liver and blood vessels. The two main forms are autosomal dominant PKD (ADPKD), which usually develops in adulthood, and autosomal recessive PKD (ARPKD), which often presents during infancy or childhood.
Timely diagnosis and regular monitoring can help detect high blood pressure, declining kidney function, increasing kidney volume and other complications. In adults with ADPKD who are at risk of rapid disease progression, appropriate assessment can help identify patients who may benefit from disease-modifying treatment such as tolvaptan. Early management of blood pressure and other complications can also help protect kidney function.
Causes
Risk Factors
Advances in polycystic kidney disease management include improved imaging, genetic assessment and methods to predict disease progression. In adults with ADPKD, MRI can help measure total kidney volume and support risk assessment, while genetic testing may help clarify the diagnosis and inform family counselling in selected cases. Treatment decisions increasingly consider kidney-function trends, imaging findings and individual risk of progression. Research continues into additional disease-modifying therapies and biomarkers that may help slow cyst growth and kidney-function decline. The availability of specialised imaging, genetic services and newer treatments varies between Malaysian healthcare centres.
Peritoneal Dialysis (PD) : PD offers excellent, continuous fluid removal, gentler blood pressure control, and fewer needle sticks, making it a popular home-based option.
Cost Start From 90Explore Options
Hemodialysis (HD) : Hemodialysis allows for aggressive fluid removal during sessions to help manage fluid-dependent hypertension.
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Kidney Transplantation : Advanced PKD may eventually cause kidney failure. Patients with kidney failure may require hemodialysis, peritoneal dialysis or kidney transplantation depending on their medical condition and eligibility.
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MediRehab (a chain of Rehab centres, part of MediGence) provides comprehensive tele-rehabilitation services designed to support Polycystic Kidney Disease patients in Malaysia. These Services include:









Kuala Lumpur, Malaysia
Prince Court is a private medical facility in the center of Kuala Lumpur that has 277 individual beds. Our dedication is to provide you with the best treatment possible from the time you arrive until you depart, healthier and happier. We are well-known for our top-notch facilities, cutting-edge technology, and friendly customer service.

Kuala Lumpur, Malaysia
Situated at the junction of Petaling Jaya and Shah Alam, close to the Oasis Ara, Ara Damansara Medical Centre boasts a serene, luxurious ambiance.
The Centre has been awarded several prestigious awards such as the Global Health Asia Pacific Awards 2023, Newsweek Best Specialized Hospital APAC 2023, Healthcare Asia Awards 2023, and Malaysian Healthcare Wellness Excellence.

Kuala Lumpur, Malaysia
Subang Jaya Medical Center is renowned for pioneering radiation oncology treatments and infrastructure in Malaysia. The hospital also has a state-of-the-art Cancer Radiosurgery Centre (CRC), which is fully furnished with the latest medical technology for cancer detection, monitoring, and treatment.
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Hematologist
9 Years of Experience
Dr. Akash Khandelwal is a distinguished Hematologist, Hemato-oncologist, and Bone Marrow Transplant (BMT) Physician with extensive training from the prestigious AIIMS New Delhi. His expertise encompasses a wide range of specialized techniques in bone marrow transplantation, including autologous and allogeneic transplants such as matched sibling donors, matched unrelated donors (MUD), and haploidentical donor transplants. Dr. Khandelwal has personally supervised and conducted over 100 bone marrow transplants. View More
Last Reviewed - January 2026