Pediatric Primary Ciliary Dyskinesia (PCD) Care

Get PCD testing and comprehensive, supportive care from our pediatric primary ciliary dyskinesia team.
Pediatric Primary Ciliary Dyskinesia (PCD) Care

On this page

Why choose UCSF Benioff Children's Hospitals for PCD care?

Pediatric primary ciliary dyskinesia (PCD) is a rare genetic condition affecting the lungs, airways and sinuses. At UCSF Benioff Children's Hospitals, we help children with PCD and their families manage symptoms and access supportive therapies.

We offer PCD testing to confirm a suspected diagnosis. If your child has PCD, our multispecialty team provides a comprehensive treatment plan to slow disease progression and support your child's growth and development.

As part of the PCD Foundation Clinical and Research Centers Network (PCDF-CRCN), we offer our patients access to PCD clinical trials evaluating promising new therapies.

Our pediatric primary ciliary dyskinesia (PCD) program

PCD affects cilia, the hair cells in the lungs and sinuses. When the cilia don't move as they should, mucus and bacteria clog the airway. PCD leads to infections in the lungs, ears and sinuses. Children may have a cough that doesn't go away and frequent nasal congestion, often starting in infancy.

Children with PCD get close monitoring and attentive care at UCSF Benioff Children's Hospitals. Our team offers PCD testing, regular assessments and personalized treatment plans to slow disease progression and help your child feel their best.

Your child's care team includes PCD specialists and experts in:

  • Pulmonology

  • Otolaryngology (ear, nose and throat)

  • Respiratory therapy

  • Audiology

  • Genetic counseling

  • Nutrition

  • Social services

PCD testing

If your child has PCD symptoms, such as chronic lung and ear infections, your provider may recommend PCD testing. We may use several tests to confirm a diagnosis, such as:

  • Exhaled nitric oxide testing. Our pulmonary function labs have specialized equipment and pediatric training to perform this minimally invasive test, which measures the level of nitric oxide your child exhales.

  • Imaging. We view your child's lungs or other organs using an X-ray or a chest CT scan.

  • Genetic testing. This blood test looks for genetic markers of PCD so we can determine if other family members need testing or care.

  • Ciliary biopsy. We take a small tissue sample from the nose or airway to help us assess how well the cilia are working.

PCD therapies

Pediatric primary ciliary dyskinesia affects each child differently, and symptoms can change over time. Therapies focus on preventing infection and helping your child breathe easier. We personalize your child's care plan and help you integrate it into your family's routine.

Providers

Awards & achievements

Recognized nationally for excellence, we pair world-class medical expertise with compassionate care to deliver the best possible outcomes for patients.
1of4
  • U.S. News & World Report Best Children's Hospitals 2026-2027, pulmonology and lung surgery

    One of the nation's best for pulmonology & lung surgery

  • U.S. News & World Report Best Children's Hospitals 2026-2027, ranked in 11 specialties

    Ranked among the nation's best in 11 specialties

Icon

Related conditions & treatments

  • Conditions
  • Treatments
    • Clinical Trials
    • Genetic Testing
    • Pulmonary Function Tests (PFT)
    • Bronchoscopy
pencil

Accreditations & memberships

Lung care for adults

As your child gets older, they transition to a UCSF Health pulmonary expert who helps them manage PCD into adulthood.