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Hemifacial microsomia guide for parents: A roadmap from diagnosis to reconstructive surgery

Your hemifacial microsomia questions, answered

If your child has been diagnosed with hemifacial microsomia, you probably have a lot of questions about the condition and their medical treatment journey. At the Division of Plastic, Reconstructive and Oral Surgery at Children’s Hospital of Philadelphia (CHOP), we want to make sure every family has the information, support and resources they need to make the best decisions about their child’s care.

Fill out the form to access insights from two world-renowned CHOP plastic surgery experts. They answer the most common questions families have about this condition.

Hemifacial Microsomia FAQ Guide for Parents

Shaikha
Patient Story

Shaikha’s story: Multiple procedures to treat Goldenhar syndrome

Born in the United Arab Emirates, Shaikha underwent jaw surgery, surgery to fix the asymmetry of her nose and cheek, and more at CHOP. “I am so satisfied with the results,” she says.

Contact the Craniofacial Program Contact Us Learn more about the Craniofacial Program
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