Overview
Clara Hildebrandt is a Pediatrics specialist and a Medical Genetics provider in Chapel Hill, North Carolina. Dr. Hildebrandt is rated as an Advanced provider by MediFind in the treatment of Arachnodactyly. Her top areas of expertise are Ring Chromosome 18, Hypotonia, Chromosome 18p Deletion, Blepharophimosis, and Gastrostomy. Dr. Hildebrandt is currently accepting new patients.
Her clinical research consists of co-authoring 16 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Arachnodactyly.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
101 Manning Dr, Chapel Hill, NC 27514
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.
Lenox Baker Children's Hospital
I am a clinical geneticist and a pediatrician with a deep interest in undiagnosed and rare genetic disorders. I provide medical care for children and adults with chromosome 22q11.2 deletion syndrome and diagnostic evaluation for patients with symptoms and signs of genetic disorders, when evaluations have not provided a specific diagnosis. Dr. Shashi is rated as a Distinguished provider by MediFind in the treatment of Arachnodactyly. Her top areas of expertise are DiGeorge Syndrome, Hypotonia, Immune Defect due to Absence of Thymus, and Micrognathia.
Kathleen Kaiser-Rogers is a Medical Genetics provider in Chapel Hill, North Carolina. Dr. Kaiser-Rogers is rated as an Advanced provider by MediFind in the treatment of Arachnodactyly. Her top areas of expertise are Trisomy 13, Chromosome 13q Duplication, Mosaicism, and Hypotonia.
Duke Internal Medicine And Pediatrics North Durh
Aimee Chung is a primary care provider, practicing in Internal Medicine and Pediatrics in Durham, North Carolina. Dr. Chung has been practicing medicine for over 20 years and is rated as an Experienced provider by MediFind in the treatment of Arachnodactyly. Her top areas of expertise are Neurogenic Bowel, Congenital Contractural Arachnodactyly, Arachnodactyly, and Marfan Syndrome.
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
- Achard SyndromeDr. Hildebrandt isAdvanced. Learn about Achard Syndrome.
- ArachnodactylyDr. Hildebrandt isAdvanced. Learn about Arachnodactyly.
- BlepharophimosisDr. Hildebrandt isAdvanced. Learn about Blepharophimosis.
- Chromosome 18p DeletionDr. Hildebrandt isAdvanced. Learn about Chromosome 18p Deletion.
- HypotoniaDr. Hildebrandt isAdvanced. Learn about Hypotonia.
- Ring Chromosome 18Dr. Hildebrandt isAdvanced. Learn about Ring Chromosome 18.
- Experienced
- Batten DiseaseDr. Hildebrandt isExperienced. Learn about Batten Disease.
- Cat Eye SyndromeDr. Hildebrandt isExperienced. Learn about Cat Eye Syndrome.
- Centronuclear MyopathyDr. Hildebrandt isExperienced. Learn about Centronuclear Myopathy.
- CLN1 DiseaseDr. Hildebrandt isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseDr. Hildebrandt isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseDr. Hildebrandt isExperienced. Learn about CLN3 Disease.