T. Andrew Burrow MD FAAP, FACMGG
Clinical Genetics, Medical Biochemical Genetics, Pediatric Medical Genetics
Clinical and Medical Biochemical Geneticist, Professor of Pediatrics
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Arkansas Children's Hospital, UAMS Medical Center1 Children's WayLittle Rock, AR 72202
Phone+1 501-263-2621
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Summary
- Dr. Thomas Burrow is a medical geneticist in Little Rock, AR and is affiliated with multiple hospitals in the area, including Arkansas Children's Hospital and UAMS Medical Center. He received his medical degree from University of Arkansas for Medical Sciences (UAMS) College of Medicine and has been in practice 18 years. He specializes in clinical genetics, medical biochemical genetics, and pediatric medical genetics and is experienced in lysosomal storage diseases, enzyme replacement therapy, clinical genetics, medical biochemical genetics, and neurogenetics.
Education & Training
Cincinnati Children's Hospital Medical CenterFellowship, Medical Genetics and Genomics, 2009- Cincinnati Children's Hospital Medical CenterResidency, Pediatrics/Medical Genetics and Genomics, 2008
- Cincinnati Children's Hospital Medical CenterInternship, Pediatrics/Medical Genetics and Genomics, 2003 - 2004
University of Arkansas For Medical Sciences College of MedicineClass of 2003
Certifications & Licensure
OH State Medical License 2003 - 2027
AR State Medical License 2016 - 2026
KY State Medical License 2009 - 2026
OK State Medical License 2024 - 2026
American Board of Medical Genetics and Genomics Medical Biochemical Genetics
American Board of Pediatrics Pediatrics- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Awards, Honors, & Recognition
- Fellow (ACMG) American College of Medical Genetics, 2009
- Fellow (FAAP) American Academy of Pediatrics
Publications & Presentations
PubMed
- Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3.Dibyendu Dutta, Jennifer Black, Emily A Montoya, Thomas Andrew Burrow, Joseph Shieh
Journal of Medical Genetics. 2025-03-20 - 26 citationsDiagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource.Rebecca L Koch, Claudia Soler-Alfonso, Bridget T Kiely, Akihiro Asai, Ariana L Smith
Molecular Genetics and Metabolism. 2023-03-01 - 1 citationsClinical insights from Wolman disease: Evaluating infantile hepatosplenomegaly.William B Hannah, Katherine Ryan, Surekha Pendyal, T Andrew Burrow, Susan E Harley
American Journal of Medical Genetics. Part A. 2022-11-01
Journal Articles
- KCTD7 Deficiency Defines a Distinct Neurodegenerative Disorder with a Conserved Autophagy‐Lysosome DefectMarsha Pratt, Katrina Peariso, Adam L Hartman, Adolfo Garnica, Satish Agadi, Gerard T Berry, Tobias Loddenkemper, Thomas A Burrow, Pankaj B Agrawal, Annals of Neurology
Professional Memberships
- Fellow
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