Dr. Luis A. Umana
Overview
Luis Umana is a Medical Genetics specialist and a Pediatrics provider in Dallas, Texas. Dr. Umana is highly rated in 177 conditions, according to our data. His top areas of expertise are Classic Galactosemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Biotinidase Deficiency, and Argininosuccinic Aciduria.
His clinical research consists of co-authoring 16 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Graduate Institution
Residency
Specialties
Licenses
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
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- MANAGED MEDICAID PLAN
- HMO
- 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
- EPO
- POS
- PPO
- HMO
- MANAGED MEDICAID PLAN
- OTHER MEDICAID
- STATE MEDICAID
- 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
- OTHER COMMERCIAL
- EPO
- HMO
- POS
- PPO
Locations
5323 Harry Hines Blvd, Dallas, TX 75390
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.
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Frequently Asked Questions about Dr. Luis A. Umana
How do I make an appointment with Dr. Luis A. Umana?
You can book an appointment with Dr. Luis A. Umana by calling their office at 214-648-2145. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Luis A. Umana a top-rated expert for Classic Galactosemia?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Luis A. Umana is classified as an Advanced expert for Classic Galactosemia, 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. Luis A. Umana specialize in?
While Dr. Luis A. Umana is a Medical Genetics, they have specific expertise in Classic Galactosemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Biotinidase Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Luis A. Umana participate in research or clinical trials?
Yes. Dr. Luis A. Umana has published 16 articles and abstracts on conditions like Classic Galactosemia. You can view a list of Dr. Luis A. Umana's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Luis A. Umana accept my insurance?
Dr. Luis A. Umana accepts most major insurance plans, including Aetna and Anthem BCBS. We recommend calling the office directly at 214-648-2145 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
- Advanced
- 15q11.2 MicrodeletionDr. Umana isAdvanced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Umana isAdvanced. Learn about 2q37 Deletion Syndrome.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- 3p Deletion SyndromeDr. Umana isAdvanced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Umana isAdvanced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Umana isAdvanced. Learn about Aase Syndrome.
- Experienced
- 3MC SyndromeDr. Umana isExperienced. Learn about 3MC Syndrome.
- Achard SyndromeDr. Umana isExperienced. Learn about Achard Syndrome.
- AcheiropodyDr. Umana isExperienced. Learn about Acheiropody.
- AchondroplasiaDr. Umana isExperienced. Learn about Achondroplasia.
- Acid Sphingomyelinase Deficiency (ASMD)
- Acro-Pectoro-Renal Field DefectDr. Umana isExperienced. Learn about Acro-Pectoro-Renal Field Defect.