About
The PKD Foundation has invested over $2 million since 2006 for research, support, education and awareness for ARPKD, ADPKD in children, and congenital hepatic fibrosis (CHF), a disease closely associated with ARPKD. This info sheet provides helpful information for parents of children with PKD, caregivers, and physicians.
Related Resources
- 2025
- ADPKD
- Caregivers
- Complications
- Education
- Living with PKD
- Newly Diagnosed
- Polycystic Liver Disease
- Symptoms
- The Basics of PKD
- Webinar
- 2025
- ADPKD
- Caregivers
- Complications
- Diagnosis
- Education
- genetic testing
- genetics
- Living with PKD
- Newly Diagnosed
- The Basics of PKD
- Webinar
- 2023
- ADPKD
- ARPKD
- Children
- Healthcare
- Healthcare Team
- PKD Parents
- Teens and Young Adults (13-20)
- Webinar
- 2023
- ADPKD
- ARPKD
- Children
- Diet
- Healthcare Team
- Management
- Nutrition
- PKD Parents
- Webinar
- Young Children
- 2023
- ADPKD
- Caregivers
- CHF
- Children
- Congenital Hepatic Fibrosis
- PKD Parents
- PKDCON
- Webinar
- Wellness
- Young Children
- 2023
- ADPKD
- ARPKD
- Caregivers
- Children
- PKD
- PKD Parents
- PKDCON
- Webinar
- Wellness
- Young Children
- ARPKD
- Children
- Complications
- PKD Parents
- Symptoms
- Young Children
- ADPKD
- Centers of Excellence
- Education
- Healthcare Team
- Nephrologist
- PKD News
- PKD Parents
- Research