Kathryn Chatfield, MD

Noonan Syndrome, CFC, Costello (RASopathy syndromes), Vascular and Lymphatic Anomalies, Hereditary Hemorrhagic Telangiectasia (HHT, or Osler-Weber-Rendu syndrome). I also specialise in management of connective tissue disorders: Marfan syndrome, Loeys Dietz syndrome, Vascular-type Ehlers Danlos syndrome, Familial aortic aneurysm and dissection syndromes, Turner syndrome, Williams syndrome, Metabolic cardiomyopathies, familial cardiomyopathy, and familial congenital heart disease.

Care Philosophy

I provide specialized care of individuals with genetic forms of cardiovascular disease. As a Clinical Geneticist and Pediatric cardiologist, I am in a unique position to diagnose the underlying etiologies of congenital heart disease, cardiomyopathies and aortopathy in children and adolescents. I treat many children with these conditions as their cardiologist; I also serve as a resource and genetics consultant to pediatric cardiologists within our practice and in the greater Rocky Mountain region.

Specialties

Clinical Genetics and Genomics (MD)
Pediatrics
Pediatric Cardiology

Conditions & Treatments

Heart and Circulation
Aneurysms, Cardiomyopathy, Circulatory Disorders, Congenital Heart Disease, Heart Failure, Heart Valve Diseases, Vascular Malformations
Genetic Conditions and Testing

Education & Training

Medical Schools

MD, Dartmouth Medical School (2006)

Undergraduate Schools

BA, Middlebury College (VT) (1996)

Graduate Schools

PhD, Dartmouth College (2003)

Residency Program

University of Pennsylvania/Children's Hospital of Philadelphia Program (2010)

Fellowships

University of Colorado (Children's Hospital Colorado) Program (2013)

information for referring providers

Referral Contact Phone

(720) 777-6820

Clinical Interests for Referring Providers

My clinical interest is in the diagnosis and management of genetic forms of aorta, vascular and congenital heart disease. I provide specialized cardiac care for patients with the following genetic conditions: Marfan syndrome, Loeys Dietz syndrome, Vascular-type Ehlers Danlos syndrome, Familial aortic aneurysm and dissection syndromes, Turner syndrome, Williams syndrome, Noonan-spectrum and RASopathy disorders, Metabolic cardiomyopathies, familial cardiomyopathy, and familial congenital heart disease. I also staff the Vascular Anomalies and Pediatric Hereditary Hemorrhagic Telangiectasia (HHT, or Osler-Weber-Rendu syndrome) Clinics, as well as the multidisciplinary Turner Syndrome Clinic at Children's Hospital Colorado

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Practice Locations

Children's Hospital Colorado Anschutz Medical Campus

Aurora