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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.

Appointments

Our team is standing by to schedule your child’s appointment.

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

craniofacial patient

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.

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.

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