Overview
Nina Powell is a Pediatrics specialist and a Medical Genetics provider in Newark, Delaware. Dr. Powell is rated as an Experienced provider by MediFind in the treatment of Aase Syndrome. Her top areas of expertise are Microcephaly, Chromosome 13q Deletion, Increased Head Circumference, and Perlman Syndrome.
Her clinical research consists of co-authoring 12 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
Locations
4701 Ogletown Stanton Road, HGCC Suite 1340, Newark, DE 19713
4701 Ogletown Stanton Road, Suite 2200, Newark, DE 19713
1600 Rockland Road, Department Of Pediatric Genetics, Wilmington, DE 19803
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Nemours DuPont Hospital For Children
Karen Gripp is a Medical Genetics provider in Wilmington, Delaware. Dr. Gripp is rated as an Elite provider by MediFind in the treatment of Aase Syndrome. Her top areas of expertise are Costello Syndrome, RASopathies, Noonan Syndrome, and Cardiofaciocutaneous Syndrome.
Dena Matalon is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Matalon is rated as a Distinguished provider by MediFind in the treatment of Aase Syndrome. Her top areas of expertise are Campomelia Cumming Type, Microcephaly Deafness Syndrome, Coffin-Lowry Syndrome, and Nevoid Basal Cell Carcinoma Syndrome.
Rubenstein Child Health Building
Dr. Harry “Hal” Dietz is a professor of pediatrics, an associate professor of medicine and an assistant professor of neurological surgery at the Johns Hopkins University School of Medicine. He is the Victor A. McKusick Professor of Genetics and also serves as the director of the William S. Smilow Center for Marfan Syndrome Research. Recognized as the world’s leading authority on Marfan syndrome, Dr. Dietz conducted genomic mapping and research on therapeutic agents for deficiencies in the genetic protein fibrillin, which is linked to Marfan syndrome. His research contributions have made diagnosis of the condition patient-specific and accurate. He has received more than 50 national and international awards and honors, including the Antoine Marfan Award from the National Marfan Foundation and the Art of Listening Award from the American Heart Association. Dr. Dietz is an ad hoc reviewer for 19 different organizations, including the American Journal of Cardiology, the Archives of Pediatric and Adolescent Medicine, and the Journal of Clinical Investigation. Over more than two decades, Dr. Dietz has mentored 75 predoctoral and postdoctoral researchers. He has authored 282 original publications in peer-reviewed journals, 25 textbook chapters, and 239 abstracts, and has also delivered more than 440 lectures on Marfan syndrome and related genetic disorders. Dr. Dietz completed his B.S. at Duke University and received his M.D. from the SUNY Upstate School of Medicine. He completed a pediatric residency and a cardiology fellowship at Johns Hopkins University before joining the faculty in 1992. Dr. Dietz is rated as an Advanced provider by MediFind in the treatment of Aase Syndrome. His top areas of expertise are Caudal Duplication, Neu Laxova Syndrome, Early Infantile Epileptic Encephalopathy, and Cardiomyopathy Hypogonadism Metabolic Anomalies.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- 15q11.2 MicrodeletionDr. Powell isAdvanced. Learn about 15q11.2 Microdeletion.
- 3MC SyndromeDr. Powell isAdvanced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Powell isAdvanced. Learn about 3p Deletion Syndrome.
- AcalvariaDr. Powell isAdvanced. Learn about Acalvaria.
- AnencephalyDr. Powell isAdvanced. Learn about Anencephaly.
- Autism Spectrum DisorderDr. Powell isAdvanced. Learn about Autism Spectrum Disorder.
- Experienced
- 2q37 Deletion SyndromeDr. Powell isExperienced. Learn about 2q37 Deletion Syndrome.
- 47 XYY SyndromeDr. Powell isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Powell isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Powell isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acro-Pectoro-Renal Field DefectDr. Powell isExperienced. Learn about Acro-Pectoro-Renal Field Defect.
- AcrocephalopolydactylyDr. Powell isExperienced. Learn about Acrocephalopolydactyly.

