Condition
Pediatric Crouzon Syndrome
What You Need to Know
Crouzon syndrome is a rare birth defect that causes premature closing of several joints in a baby’s skull.Key Symptoms
Children with Crouzon syndrome may have one or more symptoms including misshapen head, bulging, wide-set eyes, or other characteristics.
Diagnosis
At Children’s National Hospital, our pediatric team uses X-rays, diagnostic imaging and genetic tests to diagnosis Crouzon syndrome.
Treatment
Treatment for Crouzon syndrome focuses on reducing pressure inside the skull, correcting the skull and facial deformities, and ensuring proper breathing.
Frequently Asked Questions
What is Crouzon syndrome?
What causes Crouzon syndrome in children?
What are the symptoms of Crouzon syndrome in children?
How is Crouzon syndrome diagnosed in children?
How is Crouzon syndrome treated in children?
Meet the Providers Who Treat Crouzon Syndrome
Departments that Treat Crouzon Syndrome
Rare Disease Institute - Genetics and Metabolism
Children's National Rare Disease Institute (CNRDI) is a first-of-its-kind center focused exclusively on advancing the care and treatment of children and adults with rare genetic diseases.
Cleft and Craniofacial Program
The Cleft and Craniofacial Program at Children's National brings together experts from 10 pediatric disciplines to provide complete care for children with craniofacial disorders. Our multidisciplinary pediatric team helps more than 400 children every year.