Condition
Pediatric Skeletal Dysplasias
What You Need to Know
Skeletal dysplasia describes a category of rare genetic disorders that affect bones and joints and hinder children’s growth and development. The disorder causes abnormally shaped bones, especially in the head, spine and long bones of the arms and legs.
Key Symptoms
The most common symptoms of skeletal dysplasia are:
- Short stature or slow growth
- Disproportionately large head, especially the forehead
- Disproportionately short upper arms and thighs
Diagnosis
Doctors typically diagnose skeletal dysplasia by:
- X-ray
- MRI
- CT scan
- Prenatal ultrasound
- Genetic testing
Treatment
Treatment may include:
- Growth hormones
- Physical therapy
- Back braces
- Surgery
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Frequently Asked Questions
What causes skeletal dysplasia?
Types of skeletal dysplasia
Symptoms of skeletal dysplasia
How is skeletal dysplasia diagnosed?
Treatments for skeletal dysplasia
Additional resources
Meet the Providers Who Treat Skeletal Dysplasias
Departments that Treat Skeletal Dysplasias

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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