Condition
Pediatric Carpenter Syndrome
What is Carpenter Syndrome?
Carpenter syndrome is an extremely rare congenital (present at birth) disorder that causes abnormal growth of a baby’s skull, fingers, and toes. Babies born with Carpenter syndrome have skull bones that fuse too early and webbed, unusually short, or extra fingers and toes.
Frequently Asked Questions
What causes Carpenter syndrome in children?
What are the symptoms of Carpenter syndrome in children?
How is Carpenter syndrome diagnosed in children?
How is Carpenter Syndrome treated in children?
- Helping Maddie to Live Life to the Fullest
Maddie is a lively, creative teen who loves to act. Research at Children's National Hospital helps to ensure that her rare disease doesn"t upstage her big theater plans or her love of life.
Departments that Treat Carpenter Syndrome
Rare Disease Institute
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.