Early-Stage Investigator Spotlight: Chaya Nautiyal Murali Gets Creative with Osteogenesis Imperfecta Research Dakota Campbell Tue, 11/09/2021 - 13:32
Headshot of Chaya Nautiyal Murali, MD

Chaya Nautiyal Murali, MD, is a pediatric geneticist at Baylor College of Medicine and a member of the Brittle Bone Disorders Consortium (BBDC). She is also an accomplished essayist, using her creative writing skills to highlight themes of identity, inheritance, and family through the lenses of immigration and genetics. Here, she shares her start in rare disease research, exciting discoveries, and future goals.

Consortium Spotlight: Advancing Discoveries in Brittle Bone Disorders Dakota Campbell Wed, 11/03/2021 - 11:58
Members of the Brittle Bone Disorders Consortium

The Brittle Bone Disorders Consortium (BBDC) brings together physicians, researchers, and educators to learn more about osteogenesis imperfecta (OI), a genetic disorder that mainly affects the development of the bones. The goal is to develop new and better treatments for patients with OI. Here, principal investigator Brendan Lee, MD, PhD, and Vernon Sutton, MD, share the history of the consortium, current research, and future plans.

Exploring Oral Health-Related Quality of Life in Children with Osteogenesis Imperfecta Dakota Campbell Wed, 08/26/2020 - 13:52
Zoe Fang, an osteogenesis imperfecta (OI) patient, at an arcade
Zoe Fang, an osteogenesis imperfecta (OI) patient, at an arcade

In a new study, researchers in the Rare Diseases Clinical Research Network’s Brittle Bone Disorders Consortium (BBD) surveyed adolescents with osteogenesis imperfecta (OI) to learn about their oral symptoms and how these affect their quality of life. Participants’ answers are clarifying the oral health needs of kids with OI and guiding future research for orthodontic interventions.