Dr. Dwight D. Koeberl
Overview
My practice includes caring for children and adults with inherited conditions, such as inherited disorders of metabolism, genetic syndromes, mitochondrial disorders, inherited causes of growth failure or developmental delay, and conditions detected by newborn screening. My clinic works with the Pediatric Biochemical Genetics Laboratory to diagnose these conditions. We provide treatment for inherited disorders of metabolism. I work closely with the geneticists, neurologists, pediatricians, internists, and other providers at Duke University Medical Center to provide comprehensive care for my patients. My research has been aimed at developing new treatments for inherited conditions, focusing on glycogen storage diseases, like Pompe disease and von Gierke disease. We have developed gene therapy for these conditions and are in the process of starting clinical trials to test safety and benefits.
Dr. Koeberl is rated as a Distinguished provider by MediFind in the treatment of Propionic Acidemia. His top areas of expertise are Pompe Disease, Von Gierke Disease, X-Linked Creatine Deficiency, and Propionic Acidemia.
His clinical research consists of co-authoring 105 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 3 articles in the study of Propionic Acidemia.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- HMO
- POS
- 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
2301 Erwin Rd, Durham, NC 27710
3000 Erwin Rd, Durham, NC 27705
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.
2 Clinical Trials
University Of North Carolina At Chapel Hill
Clara Hildebrandt is a Pediatrics specialist and a Medical Genetics provider in Chapel Hill, North Carolina. Dr. Hildebrandt has been practicing medicine for over 10 years and is rated as an Advanced provider by MediFind in the treatment of Propionic Acidemia. Her top areas of expertise are Ring Chromosome 18, Hypotonia, Chromosome 18p Deletion, Blepharophimosis, and Gastrostomy. Dr. Hildebrandt is currently accepting new patients.
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
- Elite
- Pompe DiseaseDr. Koeberl isElite. Learn about Pompe Disease.
- Distinguished
- Propionic AcidemiaDr. Koeberl isDistinguished. Learn about Propionic Acidemia.
- Von Gierke DiseaseDr. Koeberl isDistinguished. Learn about Von Gierke Disease.
- X-Linked Creatine DeficiencyDr. Koeberl isDistinguished. Learn about X-Linked Creatine Deficiency.
- Advanced
- CitrullinemiaDr. Koeberl isAdvanced. Learn about Citrullinemia.
- Classic GalactosemiaDr. Koeberl isAdvanced. Learn about Classic Galactosemia.
- Coenzyme Q Cytochrome C Reductase Deficiency
- Galactose Epimerase DeficiencyDr. Koeberl isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Koeberl isAdvanced. Learn about Galactosemia.
- Glycogen Storage Disease Type 0Dr. Koeberl isAdvanced. Learn about Glycogen Storage Disease Type 0.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Alternating Hemiplegia of ChildhoodDr. Koeberl isExperienced. Learn about Alternating Hemiplegia of Childhood.
- Autism Spectrum DisorderDr. Koeberl isExperienced. Learn about Autism Spectrum Disorder.
- HypotoniaDr. Koeberl isExperienced. Learn about Hypotonia.
- Inborn Amino Acid Metabolism DisorderDr. Koeberl isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Maple Syrup Urine DiseaseDr. Koeberl isExperienced. Learn about Maple Syrup Urine Disease.