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Specialty
Apheresis
We offer therapeutic apheresis for children and adults with a variety of conditions, including sickle cell disease, kidney disorders, neurologic conditions, cancer and graft-versus-host disease. Apheresis treatments offered include red cell exchange, therapeutic plasma exchange, leukopheresis and extra corporeal photopheresis.
Article
News You Can Use
- Nationwide Children’s Renames Center for Gene Therapy, Honoring Jerry Mendell, MD
- Elizabeth Kryszak, PhD, Honored With Excellence in Psychological Assessment Award

Blog
Inpatient Rehabilitation: Comprehensive Services to Treat the Whole Child
Comprehensive, family-centered, individually-tailored rehabilitation services are critical to patients who are recovering from a spinal cord injury, traumatic or non-traumatic brain injury, stroke, neurological disorder, severe illness or other potential life-altering event.

Specialty
Center for Complex Craniofacial Disorders
Whether your child is diagnosed with jaw abnormalities, facial trauma, craniosynostosis, plagiocephaly or Pierre Robin syndrome, our center offers a comprehensive and compassionate approach to care, provided by experts who understand how children grow and heal.

Specialty
Single Ventricle Program
Our program is dedicated to helping children and families cope with the challenges of a single ventricle diagnosis and improve outcomes. The Heart Center is among only a handful of centers in North America that offer this dedicated service.

Specialty
Intracranial Hypertension Clinic
The recognition of idiopathic intracranial hypertension in children has increased dramatically. We are leading the response to this trend with the development of a multidisciplinary clinic for the specialized diagnosis, treatment and ongoing care of these unique children.

Specialty
Cerebral Palsy Program
Our program emphasizes excellence in clinical care while focusing on international research to improve therapies for children and adults. Our interdisciplinary team works with parents to build a family-centered patient care plan.

Condition
Emery-Dreifuss Muscular Dystrophy
Emery-Dreifuss muscular dystrophy is a rare form of MD that affects only males. Symptoms may begin in childhood or adolescence. The condition causes slowly progressive weakness in the muscles of the shoulders, upper arms, and lower legs and joint stiffness.
Limb-Girdle Muscular Dystrophy
Limb-Girdle muscular dystrophy affects males and females. Most commonly it causes progressive hip and shoulder muscle weakness that spreads to the arms, legs and back. Symptoms usually begin between ages 8 and 15 and progress slowly. Patients usually become confined to a wheelchair by age 30.
Article
Differentiating Craniosynostosis from Positional Plagiocephaly
The number of infants with head shape deformities has risen over the past several years, likely due to increased awareness of the “Back to Sleep” program. Early diagnosis and treatment of craniosynostosis can improve outcomes and reduce possible adverse effects on brain development.