Overview
Qin Sun is a Medical Genetics provider in Houston, Texas. Dr. Sun is rated as an Experienced provider by MediFind in the treatment of Pyruvate Decarboxylase Deficiency. His top areas of expertise are Purine Nucleoside Phosphorylase Deficiency, Molybdenum Cofactor Deficiency (MoCD), Urea Cycle Disorders (UCD), and Hartnup Disease.
His clinical research consists of co-authoring 62 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 1 article in the study of Pyruvate Decarboxylase Deficiency.
Insurance
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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.
Nicola Brunetti-Pierri is a Pediatrics specialist and a Medical Genetics provider in Houston, Texas. Dr. Brunetti-Pierri is rated as an Elite provider by MediFind in the treatment of Pyruvate Decarboxylase Deficiency. His top areas of expertise are Pyruvate Decarboxylase Deficiency, Crigler-Najjar Syndrome, Rotor Syndrome, and Pyruvate Dehydrogenase Deficiency.
Texas Childrens Physician Group
Brendan Lee is a Medical Genetics specialist and a Pediatrics provider in Houston, Texas. Dr. Lee is rated as an Elite provider by MediFind in the treatment of Pyruvate Decarboxylase Deficiency. His top areas of expertise are Argininosuccinic Aciduria, Urea Cycle Disorders (UCD), Osteogenesis Imperfecta, and Spondyloepimetaphyseal Dysplasia Strudwick Type. Dr. Lee is currently accepting new patients.
Baylor College Of Medicine
Fernando Scaglia is a Pediatrics specialist and a Medical Genetics provider in Houston, Texas. Dr. Scaglia is rated as a Distinguished provider by MediFind in the treatment of Pyruvate Decarboxylase Deficiency. His top areas of expertise are MELAS Syndrome, Hypotonia, Primary Carnitine Deficiency, and Leigh Syndrome. Dr. Scaglia 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
- Distinguished
- Molybdenum Cofactor Deficiency (MoCD)Dr. Sun isDistinguished. Learn about Molybdenum Cofactor Deficiency (MoCD).
- Purine Nucleoside Phosphorylase Deficiency
- Urea Cycle Disorders (UCD)Dr. Sun isDistinguished. Learn about Urea Cycle Disorders (UCD).
- Advanced
- Argininosuccinic AciduriaDr. Sun isAdvanced. Learn about Argininosuccinic Aciduria.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- CitrullinemiaDr. Sun isAdvanced. Learn about Citrullinemia.
- GABA-Transaminase Deficiency
- Hartnup DiseaseDr. Sun isAdvanced. Learn about Hartnup Disease.
- Experienced
- Cholesteryl Ester Storage DiseaseDr. Sun isExperienced. Learn about Cholesteryl Ester Storage Disease.
- Kearns-Sayre SyndromeDr. Sun isExperienced. Learn about Kearns-Sayre Syndrome.
- Leigh SyndromeDr. Sun isExperienced. Learn about Leigh Syndrome.
- Lysosomal Acid Lipase DeficiencyDr. Sun isExperienced. Learn about Lysosomal Acid Lipase Deficiency.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Progressive External Ophthalmoplegia