Overview
Brendan Lee is a Medical Genetics specialist and a Pediatrics provider in Houston, Texas. Dr. Lee is rated as an Experienced provider by MediFind in the treatment of Schwartz-Jampel Syndrome. His top areas of expertise are Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, Inborn Amino Acid Metabolism Disorder, and Urea Cycle Disorders (UCD). Dr. Lee is currently accepting new patients.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Locations
6651 Main St, Houston, TX 77030
Lindsay Burrage is a Medical Genetics specialist and a Pediatrics provider in Houston, Texas. Dr. Burrage is rated as a Distinguished provider by MediFind in the treatment of Schwartz-Jampel Syndrome. Her top areas of expertise are Urea Cycle Disorders (UCD), Hypotonia, Argininosuccinic Aciduria, and Achalasia Microcephaly Syndrome. Dr. Burrage is currently accepting new patients.
Jacqueline Hecht is a Medical Genetics provider in Houston, Texas. Dr. Hecht is rated as a Distinguished provider by MediFind in the treatment of Schwartz-Jampel Syndrome. Her top areas of expertise are Pseudoachondroplasia, Achondroplasia, Cleft Lip and Palate, Adenoidectomy, and Myringotomy.
Carlos Bacino is a Pediatrics specialist and a Medical Genetics provider in Houston, Texas. Dr. Bacino is rated as an Elite provider by MediFind in the treatment of Schwartz-Jampel Syndrome. His top areas of expertise are Achondroplasia, Angelman Syndrome, Miller-Dieker Syndrome, and Lissencephaly 1. Dr. Bacino 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
- Ornithine Transcarbamylase Deficiency
- Ornithine Translocase Deficiency
- Experienced
- Arginase DeficiencyDr. Lee isExperienced. Learn about Arginase Deficiency.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Inborn Amino Acid Metabolism Disorder
- N-Acetylglutamate Synthase Deficiency
- Urea Cycle Disorders (UCD)Dr. Lee isExperienced. Learn about Urea Cycle Disorders (UCD).