Overview
Dena Matalon is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Matalon is rated as an Experienced provider by MediFind in the treatment of Lissencephaly 1. Her top areas of expertise are Campomelia Cumming Type, Microcephaly Deafness Syndrome, Coffin-Lowry Syndrome, and Nevoid Basal Cell Carcinoma Syndrome.
Her clinical research consists of co-authoring 25 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
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.
Mahim Jain is a Medical Genetics specialist and a Pediatrics provider in Wilmington, Delaware. Dr. Jain is rated as a Distinguished provider by MediFind in the treatment of Lissencephaly 1. His top areas of expertise are Osteogenesis Imperfecta, Spondyloepimetaphyseal Dysplasia Strudwick Type, Miller-Dieker Syndrome, and Lissencephaly 1. Dr. Jain is currently accepting new patients.
Nemours DuPont Hospital For Children
Laura Owens is a Pediatrics provider in Wilmington, Delaware. Dr. Owens is rated as an Advanced provider by MediFind in the treatment of Lissencephaly 1. Her top areas of expertise are Mucopolysaccharidoses (MPS), Developmental Dysphasia Familial, Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), and Bilateral Perisylvian Polymicrogyria.
Childrens Health Care Associates Inc
Christina Bergqvist is a Pediatric Neurologist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Bergqvist is rated as an Advanced provider by MediFind in the treatment of Lissencephaly 1. Her top areas of expertise are Lennox-Gastaut Syndrome (LGS), Dihydrolipoamide Dehydrogenase Deficiency, Pyruvate Carboxylase Deficiency, and Autosomal Recessive Congenital Methemoglobinemia.
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
- Distinguished
- Campomelia Cumming TypeDr. Matalon isDistinguished. Learn about Campomelia Cumming Type.
- Coffin-Lowry SyndromeDr. Matalon isDistinguished. Learn about Coffin-Lowry Syndrome.
- Microcephaly Deafness SyndromeDr. Matalon isDistinguished. Learn about Microcephaly Deafness Syndrome.
- Advanced
- 15q11.2 MicrodeletionDr. Matalon isAdvanced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Matalon isAdvanced. Learn about 2q37 Deletion Syndrome.
- 3MC SyndromeDr. Matalon isAdvanced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Matalon isAdvanced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Matalon isAdvanced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Matalon isAdvanced. Learn about Aase Syndrome.
- Experienced
- Achalasia Microcephaly SyndromeDr. Matalon isExperienced. Learn about Achalasia Microcephaly Syndrome.
- AchondroplasiaDr. Matalon isExperienced. Learn about Achondroplasia.
- Acro-Pectoro-Renal Field DefectDr. Matalon isExperienced. Learn about Acro-Pectoro-Renal Field Defect.
- Acrofrontofacionasal Dysostosis SyndromeDr. Matalon isExperienced. Learn about Acrofrontofacionasal Dysostosis Syndrome.
- Acromicric DysplasiaDr. Matalon isExperienced. Learn about Acromicric Dysplasia.
- Acropectoral SyndromeDr. Matalon isExperienced. Learn about Acropectoral Syndrome.