Overview
Garrett Gotway is a Pediatrics specialist and a Medical Genetics provider in Dallas, Texas. Dr. Gotway is rated as an Experienced provider by MediFind in the treatment of Chromosome 15q Deletion. His top areas of expertise are Bardet-Biedl Syndrome, Cockayne Syndrome Type 1, Athabaskan Brain Stem Dysgenesis, and Yunis-Varon Syndrome.
His clinical research consists of co-authoring 21 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:
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
- EPO
- HMO
- PPO
- MANAGED MEDICAID PLAN
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- MANAGED MEDICAID PLAN
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- 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.
Angela Scheuerle is a Pediatrics specialist and a Medical Genetics provider in Dallas, Texas. Dr. Scheuerle is rated as a Distinguished provider by MediFind in the treatment of Chromosome 15q Deletion. Her top areas of expertise are Hennekam Syndrome, Fetal Akinesia Sequence, Hemihyperplasia, and Incontinentia Pigmenti.
Luis Umana is a Pediatrics specialist and a Medical Genetics provider in Dallas, Texas. Dr. Umana is rated as an Advanced provider by MediFind in the treatment of Chromosome 15q Deletion. His top areas of expertise are Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Classic Galactosemia, Biotinidase Deficiency, and 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.
Cook Childrens Physician Network
Mary Kukolich is a Medical Genetics specialist and a Pediatrics provider in Ft Worth, Texas. Dr. Kukolich is rated as an Advanced provider by MediFind in the treatment of Chromosome 15q Deletion. Her top areas of expertise are Micrognathia, Stickler Syndrome, Kabuki Syndrome, and 3MC Syndrome. Dr. Kukolich 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
- Advanced
- 2q37 Deletion SyndromeDr. Gotway isAdvanced. Learn about 2q37 Deletion Syndrome.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- 3MC SyndromeDr. Gotway isAdvanced. Learn about 3MC Syndrome.
- 47 XYY SyndromeDr. Gotway isAdvanced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Gotway isAdvanced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Gotway isAdvanced. Learn about Abruzzo-Erickson Syndrome.
- Experienced
- 15q11.2 MicrodeletionDr. Gotway isExperienced. Learn about 15q11.2 Microdeletion.
- 3p Deletion SyndromeDr. Gotway isExperienced. Learn about 3p Deletion Syndrome.
- Achard SyndromeDr. Gotway isExperienced. Learn about Achard Syndrome.
- Acro-Pectoro-Renal Field DefectDr. Gotway isExperienced. Learn about Acro-Pectoro-Renal Field Defect.
- AcrocephalopolydactylyDr. Gotway isExperienced. Learn about Acrocephalopolydactyly.
- Acromegaloid Facial Appearance SyndromeDr. Gotway isExperienced. Learn about Acromegaloid Facial Appearance Syndrome.