The Cunningham Lab investigates the mechanisms behind craniosynostosis and other malformations. Our goal is to make discoveries that lead to better care for patients with craniofacial conditions.
Unraveling the Causes of Craniosynostosis
Craniosynostosis is a hereditary condition that occurs when the sutures, or seams, between a child’s skull bones fuse too early. This stops the skull from expanding as the brain grows. Craniosynostosis can lead to an abnormally-shaped head, increased pressure inside the skull, facial malformations and other problems. Most children with craniosynostosis need extensive surgery.
Our craniosynostosis research focuses on understanding single-suture craniosynostosis (SSC), which occurs when only one suture is prematurely fused. This occurs in approximately one in 2,500 births.
Single-Suture Craniosynostosis Gene Expression and Discovery
We work with researchers in the University of Washington Department of Genome Sciences to identify mutations and altered genetic pathways that cause craniosynostosis. Using next-generation sequencing, gene expression studies and cell biology, our team is identifying molecular risks for developing SSC. This will enhance our ability to counsel patients and families, and holds great promise for identifying biological pathways that could be modified to treat and perhaps prevent craniosynostosis.
Read a detailed abstract from the NIH’s RePORT website.
Neurobehavioral Correlates of Craniosynostosis
We collaborated with Dr. Matt Speltz on the first large study to track neurodevelopment in children with SSC from infancy until elementary school. While Children with SSC had higher rates of learning problems than children without SSC, those issues were usually mild enough that they could be treated with standard interventions like tutoring and special education. Our results could spur craniofacial programs to improve developmental screening for children with SSC.
Read the study’s findings in the journal Pediatrics.
Identifying genes that cause rare craniofacial malformations
Working with the University of Washington Department of Genome Sciences, we use candidate gene analysis, gene expression studies and next-generation sequencing to identify the genetic causes of rare craniofacial conditions, including auriculo-condylar syndrome, acromelic frontonasal dysplasia, Mercedes synostosis and oculo-oto-facial dysplasia.
This has immediate benefits for patients and families, including improved genetic counseling and family planning. These discoveries also fuel our developmental biology research to identify biologic variations that can be targeted for improved treatments.
Harnessing the Power of Collaboration
Our lab’s highly collaborative nature brings researchers with different specialties together to investigate all facets of craniofacial conditions. We work side by side with other researchers and clinicians in Seattle Children’s Craniofacial Center, and at the University of Washington, Sage Bionetworks and other institutions. This helps us build a comprehensive understanding of these disorders. Our long-term goal is to translate this knowledge into diagnostic tools, therapies and techniques that improve the lives of patients and their families.
Support Craniofacial Research at Seattle Children’s
The Cunningham Lab and Seattle Children’s Craniofacial Center are poised to make important discoveries that will help improve care of children with craniosynostosis, cleft lip and palate, craniofacial microsomia and other conditions affecting hundreds of thousands of patients worldwide. Much of the center’s success in research and in obtaining federal funding is due to pilot research projects funded through philanthropy. Consider making a donation to craniofacial research.