Overview
Ryan Gates is a Medical Genetics specialist and a Pediatrics provider in Fort Worth, Texas. Dr. Gates is rated as an Experienced provider by MediFind in the treatment of Hypomelanosis of Ito. His top areas of expertise are Micrognathia, Von Gierke Disease, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Neu Laxova Syndrome. Dr. Gates is currently accepting new patients.
His clinical research consists of co-authoring 1 peer reviewed article. 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
Accepted plan types not found. Please verify directly with the provider.
- EPO
- HMO
- 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.
Garrett Gotway is a Pediatrics specialist and a Medical Genetics provider in Dallas, Texas. Dr. Gotway is rated as an Advanced provider by MediFind in the treatment of Hypomelanosis of Ito. His top areas of expertise are Bardet-Biedl Syndrome, Cockayne Syndrome Type 1, Athabaskan Brain Stem Dysgenesis, and Yunis-Varon Syndrome.
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 Hypomelanosis of Ito. 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 Hypomelanosis of Ito. 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.
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
- MicrognathiaDr. Gates isAdvanced. Learn about Micrognathia.
- Experienced
- 15q11.2 MicrodeletionDr. Gates isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Gates isExperienced. Learn about 2q37 Deletion Syndrome.
- 3p Deletion SyndromeDr. Gates isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Gates isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Gates isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Gates isExperienced. Learn about Abruzzo-Erickson Syndrome.