The 20 Best Noonan Syndrome Doctors Near Me in District of Columbia, US
Find the Top Noonan Syndrome Experts and Specialists
Kaiser Permanente Capitol Hill Medical Center
Jason Mitchell is a Pediatric Cardiologist practicing medicine in Washington, Washington, D.c.. Dr. Mitchell is rated as an Experienced provider by MediFind in the treatment of Noonan Syndrome. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Heart Murmurs, Patent Ductus Arteriosus, Ventricular Septal Defects, and Dextrocardia with Situs Inversus.
Office
Nicolas Cuttriss is a Pediatric Endocrinologist practicing medicine in Washington, Washington, D.c.. Dr. Cuttriss is rated as an Experienced provider by MediFind in the treatment of Noonan Syndrome. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Type 1 Diabetes (T1D), Short Stature (Growth Disorders), Idiopathic Short Stature (ISS), and Familial Short Stature (FSS).
Patroula Smpokou is a Medical Genetics provider practicing medicine in Washington, Washington, D.c.. Dr. Smpokou is rated as an Advanced provider by MediFind in the treatment of Noonan Syndrome. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses RASopathies, Noonan Syndrome, Lhermitte-Duclos Disease, and Bannayan-Riley-Ruvalcaba Syndrome.
Telehealth Video Visit
Andrew Dauber, MD, MMSc, is the chief of endocrinology at Children’s National Hospital. As a pediatric endocrinologist, Dr. Dauber works in all areas of pediatric endocrinology, but specializes in studying and treating growth disorders. Dr. Dauber has published more than 65 studies and regularly speaks at international pediatric endocrinology conferences, discussing a variety of topics, including clinical clues to identify rare genetic growth conditions, genetic factors that influence height and the timing of puberty, as well as novel genetic disorders that he has helped identify. He is the recipient of the 2020 Richard E. Weitzman Outstanding Early Career Investigator Award from the Endocrine Society for successfully applying innovative genetic technologies to pediatric endocrinology. With a medical degree and a Master’s of Medical Sciences in Clinical Investigation from Harvard Medical School, Dr. Dauber finds it natural to merge academic research with its clinical counterparts to accelerate cutting-edge treatment and multidisciplinary care. He is currently working with pediatric health centers to integrate genomics into patient registries and electronic health records, harnessing large data sets, including whole-exome sequences, to help clinicians identify and treat high-risk patients. Over the next few years, Dr. Dauber will create an endocrinology research program at Children’s National, transforming the type of care that children with endocrine disorders receive. This will make it easier for parents to find comprehensive resources for rare conditions, thyroid problems, growth disorders, early or delayed puberty, as well as type 1 and type 2 diabetes. Dr. Dauber also has experience with guiding joint infrastructures and engines of innovation. Previously, he served as the program director and director of translational research at the interdisciplinary Cincinnati Center for Growth Disorders at Cincinnati Children’s Hospital Medical Center. Additionally, he was the director of their Genomics First for Undiagnosed Diseases Program and guided medical residents and fellows as an associate professor of pediatrics at the University of Cincinnati. He held similar roles as the assistant medical director for the clinical research unit at Boston Children’s Hospital and as an assistant professor in pediatrics at Harvard Medical School. Dr. Dauber holds board certifications in pediatrics and pediatric endocrinology from the American Board of Pediatrics. He is an active member of and has received several awards and honors from the Endocrine Society, Pediatric Endocrine Society, European Society of Pediatric Endocrinology and the Society for Pediatric Research. Dr. Dauber is rated as an Experienced provider by MediFind in the treatment of Noonan Syndrome. He is also highly rated in 17 other conditions, according to our data. His clinical expertise encompasses Short Stature (Growth Disorders), Hypochondroplasia, Precocious Puberty, and Growth Hormone Deficiency (GHD). Dr. Dauber is board certified in Endocrinology Diabetes And Metabolism: American Board Of Pediatrics, 2011 and Pediatrics: American Board Of Pediatrics, 2007.
Main Hospital-Diabetes Complex Clinic
Priya Vaidyanathan, MD, is a board-certified pediatric endocrinologist who has been on the staff of the Children's National Hospital since December 2005 soon after completing her pediatric endocrinology fellowship. She provides clinical care to patients with diverse endocrine needs, and her research interest is in the field of thyroid disorders. Dr. Vaidyanathan is rated as an Experienced provider by MediFind in the treatment of Noonan Syndrome. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Short Stature (Growth Disorders), Type 1 Diabetes (T1D), Diabetes Insipidus (DI), and Neurohypophyseal Diabetes Insipidus. Dr. Vaidyanathan is board certified in Pediatric Endocrinology: American Board Of Pediatrics, 2007 and Pediatrics: American Board Of Pediatrics, 2002.
Main Hospital-Genetics Clinic
Christina Grant, MD, PhD, completed her medical genetics and medical biochemical genetics training at the National Institutes of Health National Human Genome Research Institute in Bethesda, MD, and joined Children’s National Hospital in 2018. Her clinical and research interests focus on large molecule storage disorders especially lysosomal storage diseases. Dr. Grant is rated as an Experienced provider by MediFind in the treatment of Noonan Syndrome. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A), and Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome). Dr. Grant is board certified in Medical Biochemical Genetics: American Board Of Medical Genetics And Genomics, 2019, American Board Of Medical Genetics And Genomics, 2017, and Pediatrics: American Board Of Pediatrics, 2015.
Telehealth Video Visit
Andrea Estrada is a Pediatric Endocrinologist practicing medicine in Washington, Washington, D.c.. She has been practicing medicine for over 17 years. Dr. Estrada is rated as an Experienced provider by MediFind in the treatment of Noonan Syndrome. She is also highly rated in 6 other conditions, according to our data. Her clinical expertise encompasses Mccune-Albright Syndrome, Osteitis Fibrosa, Albright's Hereditary Osteodystrophy, and Pseudohypoparathyroidism. Dr. Estrada is board certified in Pediatric Endocrinology: American Board Of Pediatrics, 2015 and Pediatrics: American Board Of Pediatrics, 2012.
Dina Zand is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Washington, Washington, D.c.. Dr. Zand is rated as an Experienced provider by MediFind in the treatment of Noonan Syndrome. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses Agyria Pachygyria Polymicrogyria, Cerebellar Hypoplasia, Lissencephaly 1, and Miller-Dieker Syndrome.
Howard University
Gail Nunlee is a Pediatric Endocrinologist and a Pediatrics provider practicing medicine in Washington, Washington, D.c.. Dr. Nunlee is rated as an Experienced provider by MediFind in the treatment of Noonan Syndrome. She is also highly rated in 14 other conditions, according to our data. Her clinical expertise encompasses Type 2 Diabetes (T2D), Graves Disease, Maturity Onset Diabetes of the Young, and Type 1 Diabetes (T1D).
To see more doctors, please expand your search radius or view related conditions below.
Last Updated: 06/30/2026



