Overview
Sarah Elsea is a Medical Genetics provider practicing medicine in Houston, Texas.
Dr. Elsea is highly rated in 14 conditions, according to our data. Her clinical expertise encompasses Smith-Magenis Syndrome, Potocki-Lupski Syndrome, Hypotonia, and Zellweger Syndrome.
She is actively involved in clinical research, co-authoring 146 peer reviewed articles.
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Insurance
Accepted insurance can change. Please verify directly with the provider.
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.
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Lorraine Potocki is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Houston, Texas. Dr. Potocki is highly rated in 10 conditions, according to our data. Her clinical expertise encompasses Potocki-Lupski Syndrome, Smith-Magenis Syndrome, Hypotonia, and Trisomy 17 Mosaicism. Dr. Potocki is currently accepting new patients.
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Frequently Asked Questions about Dr. Sarah H. Elsea
How do I make an appointment with Dr. Sarah H. Elsea?
You can book an appointment with Dr. Sarah H. Elsea by calling their office at 713-798-5484. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Sarah H. Elsea a top-rated expert for Smith-Magenis Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Sarah H. Elsea is classified as an Elite expert for Smith-Magenis Syndrome, 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. Sarah H. Elsea specialize in?
While Dr. Sarah H. Elsea is a Medical Genetics, they have specific expertise in Smith-Magenis Syndrome, Potocki-Lupski Syndrome, and Hypotonia. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Sarah H. Elsea participate in research or clinical trials?
Yes. Dr. Sarah H. Elsea has published 146 articles and abstracts on conditions like Smith-Magenis Syndrome. You can view a list of Dr. Sarah H. Elsea's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- HypotoniaDr. Elsea isElite. Learn about Hypotonia.
- Potocki-Lupski SyndromeDr. Elsea isElite. Learn about Potocki-Lupski Syndrome.
- Smith-Magenis SyndromeDr. Elsea isElite. Learn about Smith-Magenis Syndrome.
- Distinguished
- Urea Cycle Disorders (UCD)Dr. Elsea isDistinguished. Learn about Urea Cycle Disorders (UCD).
- Zellweger SyndromeDr. Elsea isDistinguished. Learn about Zellweger Syndrome.
- Advanced
- Achalasia Microcephaly SyndromeDr. Elsea isAdvanced. Learn about Achalasia Microcephaly Syndrome.
- Argininosuccinic AciduriaDr. Elsea isAdvanced. Learn about Argininosuccinic Aciduria.
- Autism Spectrum DisorderDr. Elsea isAdvanced. Learn about Autism Spectrum Disorder.
- BrachydactylyDr. Elsea isAdvanced. Learn about Brachydactyly.
- Leigh SyndromeDr. Elsea isAdvanced. Learn about Leigh Syndrome.
- MicrocephalyDr. Elsea isAdvanced. Learn about Microcephaly.
- Experienced
- AchondrogenesisDr. Elsea isExperienced. Learn about Achondrogenesis.
- Acromesomelic DysplasiaDr. Elsea isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type
- Carbamoyl Phosphate Synthetase 1 Deficiency