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Fabry disease is an inherited condition caused by a faulty gene. An enzyme the body needs to break down a certain type of fat is missing or not working properly. As a result, the fat builds up in the blood and the walls of blood vessels.
Symptoms of Fabry disease may include:
Over time the disease can lead to severe kidney and heart problems.
Doctors can treat Fabry disease with an infusion that replaces the missing enzyme.
It’s now becoming possible to diagnose Fabry disease in newborns.
Chief of Genetic and Genomic Medicine
Dr. Vockley is a global leader in inborn errors of metabolism treatment and research. He’ s also a founder of the North American Metabolic Academy.
If a doctor diagnosed your child with Fabry disease, we want you to know you're not alone. The Center for Rare Disease Therapy (CRDT) at UPMC Children's Hospital of Pittsburgh is here to help.
Here’s what you can expect when you come to us for a consult.
You can expect your first visit to take from 4 to 6 hours. Your child will receive a complete assessment from one of the center's doctors.
The doctor will make or confirm a Fabry disease diagnosis and find out how much the disease has progressed.
Because we work as a team at the center, other doctors and staff might see your child during your visit.
These may include a:
Members of your child's care team will talk with you about:
By the end of your visit, you'll have a Fabry disease care plan tailored to your child's needs. We'll also schedule a follow-up visit.
You'll meet our nurse practitioner. You can contact them by phone or video conference with any concerns before your next visit.
Before you leave, please ask us about your child's Fabry disease diagnosis, treatment, or anything else on your mind.
We'll call within 2 weeks to review the test results and the next steps for your child's Fabry disease care.
You can also find your child's test results if you have a MyCHP account — Children's patient portal.
MyCHP lets you manage your child's health online. It's free for kids getting treatment at UPMC Children's Hospital of Pittsburgh and their loved ones.
A child with a rare disease like Fabry disease affects the whole family. We see each family member as our partner at the CRDT.
The best care happens when we merge our Fabry disease expertise with your knowledge of your child's needs.
Learn how others are finding help and hope for their child’s rare disease through the expertise at UPMC Children’s.
View Center for Rare Disease Therapy patient stories »
At the CRDT, every child diagnosed with a rare disease receives a tailored treatment plan and family-centered care.
For an appointment, consult, or referral, contact us:
We’ll be in touch within 2 business days.
Children's Hospital's main campus is located in the Lawrenceville neighborhood. Our main hospital address is:
UPMC Children’s Hospital of Pittsburgh One Children’s Hospital Way 4401 Penn Ave. Pittsburgh, PA 15224
In addition to the main hospital, Children's has many convenient locations in other neighborhoods throughout the greater Pittsburgh region.
With MyCHP, you can request appointments, review test results, and more.
For questions about a hospital bill call:
To pay your bill online, please visit UPMC's online bill payment system.
Interested in giving to Children's Hospital? Support the hospital by making a donation online, joining our Heroes in Healing monthly donor program, or visiting our site to learn about the other ways you can give back.