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PRESS RELEASE

Dr Dufresne published an abstract of the first-ever clinical practice guidelines for Freeman-Burian syndrome, a rare craniofacial disorder.

Be sure to browse related website resources for more information about Dr Dufresne and do not hesitate to contact us, should you desire additional information, resources, or to schedule an interview.

Abstract of First-Ever Clinical Practice Guidelines on Rare Craniofacial Disorder Published

FOR IMMEDIATE RELEASE

Date: 01 Dec 2021

FAIRFAX—An abstract of first-ever clinical practice guidelines on Freeman-Burian syndrome (FBS) was published in the December 2021 issue of the journal, FACE. The guidelines were presented in May by Mikaela I Poling at the American Society of Craniofacial Surgeons Annual Meeting at the American Cleft Palate-Craniofacial Association Annual Meeting. Poling is Dr Craig R Dufresne’s Research Assistant. Dufresne, a Washington, DC area plastic surgeon in private practice, has written extensively about FBS and other craniofacial deformities and is considered to be one of the leading experts in the world, having cared for affected patients since the mid-1980s. Dufresne and Poling are the lead authors of the guidelines, which are expected to be published Q4 2022 or Q1 2023.

Clinical practice guidelines are used by doctors, hospitals, policymakers, and lawmakers to guide patient care, set the standard of care, determine covered services for insurance, determine needed resources and services, and help families and patients understand what care they may need. All major areas impacted by FBS are covered in these ground-breaking guidelines, including: prenatal care, delivery and neonatal care, diagnosis, primary care, dental care, craniofacial surgery, rehabilitation, psychosocial care, educational needs, and anesthesia care. The guidelines are the culmination of over a decade of work, and as a prelude to the guidelines, Dufresne previously published explanatory articles discussing evidence and experience in these areas of care.

FBS, an exceptionally rare and difficult to treat birth defect, is primarily a condition of facial and skull muscles that frequently involves muscles in the arms, legs, and elsewhere and is unique in many other ways. Without a clear understanding of FBS, how to treat affected patients, or resources needed for treatment, patient outcomes have remained relatively unchanged since its first description in the medical literature in 1938. It’s Dufresne’s hope that the new guidelines will represent a total paradigm shift and herald a new era of vastly improved patient care and research.

For Dufresne, writing about rare conditions is all about educating people—scientists, physicians, care teams, family members, and patients—in order to improve patients’ chances for a healthy, normal, and productive life. An ever-humble gentleman, publishing medical articles is his way to help many more patients than he ever could directly.

For more information and to arrange interviews with Dr Dufresne and a patient who has this very rare syndrome, please contact the office.

Craig R Dufresne, MD, PC, with offices in Fairfax, Virginia and Chevy Chase, Maryland, is a premier private solo practice providing aesthetic and reconstructive surgery care to adults and children from across the globe. Research supports the mission to provide safe, exceptional, innovative, and compassionate care that enhances overall well-being and health.

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