Overview
Heather Crawford is a Medical Genetics specialist and a Pediatrics provider in Fort Worth, Texas. Dr. Crawford is rated as an Experienced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Crawford is currently accepting new patients.
Her clinical research consists of co-authoring 8 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:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- MANAGED MEDICAID PLAN
- MANAGED MEDICAID PLAN
- MEDICARE SNP
Accepted plan types not found. Please verify directly with the provider.
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- OTHER MANAGED MEDICAID
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- EPO
- HMO
- PPO
- MANAGED MEDICAID PLAN
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- 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.
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 HNRNPH2-Related Disorder. His top areas of expertise are Bardet-Biedl Syndrome, Cockayne Syndrome Type 1, Athabaskan Brain Stem Dysgenesis, and Yunis-Varon Syndrome.
University Of Texas Southwestern Medical Center At Dallas
Saima Kayani is a Pediatric Neurologist and a Pediatrics provider in Dallas, Texas. Dr. Kayani is rated as a Distinguished provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Leigh Syndrome, CLN2 Disease, Batten Disease, and CLN3 Disease.
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 HNRNPH2-Related Disorder. 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
- Dihydropteridine Reductase DeficiencyDr. Crawford isAdvanced. Learn about Dihydropteridine Reductase Deficiency.
- Maternal HyperphenylalaninemiaDr. Crawford isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Phenylketonuria (PKU)Dr. Crawford isAdvanced. Learn about Phenylketonuria (PKU).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Campomelia Cumming TypeDr. Crawford isExperienced. Learn about Campomelia Cumming Type.
- Campomelic DysplasiaDr. Crawford isExperienced. Learn about Campomelic Dysplasia.
- Cardiofaciocutaneous SyndromeDr. Crawford isExperienced. Learn about Cardiofaciocutaneous Syndrome.
- Cardiomyopathic LentiginosisDr. Crawford isExperienced. Learn about Cardiomyopathic Lentiginosis.
- Chromosome 11 Uniparental DisomyDr. Crawford isExperienced. Learn about Chromosome 11 Uniparental Disomy.
- Chromosome 2 Uniparental DisomyDr. Crawford isExperienced. Learn about Chromosome 2 Uniparental Disomy.