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 highly rated in 7 conditions, according to our data. His top areas of expertise are Pompe Disease, Von Gierke Disease, X-Linked Creatine Deficiency, and Kearns-Sayre Syndrome.
His clinical research consists of co-authoring 106 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years.
Specialties
Licenses
Board Certifications
Fellowships
Hospital Affiliations
Languages Spoken
Gender
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
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 highly rated in 8 conditions, according to our data. Her top areas of expertise are DiGeorge Syndrome, Hypotonia, Immune Defect due to Absence of Thymus, and Micrognathia.
Duke Health Integrated Practice Inc
Priya Kishnani is a Pediatrics provider in Durham, North Carolina. Dr. Kishnani is highly rated in 11 conditions, according to our data. Her top areas of expertise are Pompe Disease, Glycogen Storage Disease Type 3, Hypophosphatasia (HPP), Glycogen Storage Disease Type 9, and Splenectomy. Dr. Kishnani is currently accepting new patients.
Duke Children's Health Center Kidney Transplant Clinic
I am a pediatric nephrologist and work with children with kidney disease. Some of the conditions that we see include congenital malformations of the kidney and the bladder, nephrotic syndrome, glomerulonephritis (inflammation of the kidney filters), and children who are on dialysis or who received kidney transplantation because of kidney failure. I listen carefully to parents when they bring their children to the clinic because they know their children better than any other person, and they are the best advocates for their child. I collaborate a lot with the other doctors in the clinic. Rest assured, when you visit our clinic and I am not around, the doctor who is seeing you knows everything about your child. This is a group practice with a very caring multidisciplinary team. Dr. Gbadegesin is highly rated in 9 conditions, according to our data. His top areas of expertise are Focal Segmental Glomerulosclerosis, Nephrotic Syndrome, Minimal Change Disease, Glomerulonephritis, and Kidney Transplant.
Frequently Asked Questions about Dr. Dwight D. Koeberl
How do I make an appointment with Dr. Dwight D. Koeberl?
You can book an appointment with Dr. Dwight D. Koeberl by calling their office at 919-684-8111. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Dwight D. Koeberl a top-rated expert for Pompe Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Dwight D. Koeberl is classified as an Elite expert for Pompe Disease, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Dwight D. Koeberl specialize in?
While Dr. Dwight D. Koeberl is a Medical Genetics, they have specific expertise in Pompe Disease, Von Gierke Disease, and X-Linked Creatine Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Dwight D. Koeberl participate in research or clinical trials?
Yes. Dr. Dwight D. Koeberl has published 106 articles and abstracts on conditions like Pompe Disease. You can view a list of Dr. Dwight D. Koeberl's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Dwight D. Koeberl accept my insurance?
Dr. Dwight D. Koeberl accepts most major insurance plans, including Aetna and Ambetter. We recommend calling the office directly at 919-684-8111 to verify that your specific plan is currently accepted before your visit.
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
- Von Gierke DiseaseDr. Koeberl isDistinguished. Learn about Von Gierke Disease.
- X-Linked Creatine DeficiencyDr. Koeberl isDistinguished. Learn about X-Linked Creatine Deficiency.
- Advanced
- Glycogen Storage Disease Type 0Dr. Koeberl isAdvanced. Learn about Glycogen Storage Disease Type 0.
- Kearns-Sayre SyndromeDr. Koeberl isAdvanced. Learn about Kearns-Sayre Syndrome.
- Mitochondrial Trifunctional Protein Deficiency
- Pyruvate Carboxylase DeficiencyDr. Koeberl isAdvanced. Learn about Pyruvate Carboxylase Deficiency.
- Experienced
- 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.
- Newborn JaundiceDr. Koeberl isExperienced. Learn about Newborn Jaundice.
- Newborn Low Blood SugarDr. Koeberl isExperienced. Learn about Newborn Low Blood Sugar.
- Urea Cycle Disorders (UCD)Dr. Koeberl isExperienced. Learn about Urea Cycle Disorders (UCD).