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Karla M. Bermudez Wagner, MD


Maternal Fetal Medicine

Contact Information

6651 Fannin Street
Suite F420
United States
Texas US

Phone: 832-826-7500

Karla M. Bermudez Wagner, MD


School Education Degree Year
Albert Einstein College of Medicine fellowship Maternal Fetal Medicine 2014
University of California San Francisco fellowship Medical Genetics 2011
Temple University Hospital residency Obstetrics & Gynecology 2009
Universidad Central de Venezuela medical school Doctor of Medicine 1996

Personal Statement

Dr. Karla Bermudez Wagner is an Assistant Professor in the Department of the Obstetrics & Gynecology at Baylor College of Medicine.  She is a Maternal-Fetal Medicine specialist who sees patients at the Texas Children Hospital Pavilion for Women. Dr. Bermudez Wagner provides consultation and comprehensive care for high-risk pregnancies with complex medical, surgical and obstetrical conditions. Her clinical interests include ultrasound, prenatal diagnosis and management of pregnancies complicated by fetal or maternal genetic disease and fetal anomalies. She performs diagnostic procedures such as chorionic villus sampling and amniocentesis. Dr. Bermudez Wagner is actively involved with the educational training of medical students, residents and fellows.
Dr. Bermudez Wagner earned her medical degree from the Universidad Central de Venezuela and completed her Obstetrics & Gynecology residency at Temple University Hospital in Philadelphia, PA. She completed her Clinical Genetics training at the University of California San Francisco, CA followed by a fellowship training in Maternal-Fetal Medicine at Albert Einstein College of Medicine in Bronx, NY. Dr. Bermudez Wagner is board certified in Obstetrics & Gynecology and in Clinical Genetics. She is an active member of the Society for Maternal Fetal Medicine and American College of Obstetrics and Gynecology. 


Organization Name Role
American College of Obstetricians and Gynecologists Member
American Institute of Ultrasound in Medicine Member
American Medical Association Member
Society for Maternal Fetal Medicine Member

Selected Publications

Bermudez-Wagner K, Jeng LJ, Slavotinek AM, Sanford EF. 2p16.3 microdeletion with partial deletion of the neurexin-1 gene in a female with developmental delays, short stature, and a congenital diaphragmatic hernia. Clinical Dysmorphology 2013 Jan;22(1):22-4. PubMed PMID: 23207424.

Sanford EF, Bermudez-Wagner K, Jeng LJ, Rauen KA, Slavotinek AM. Congenital diaphragmatic hernia in Smith-Magenis syndrome: a possible locus at chromosome 17p11.2. American Journal of Medical Genetics Part A 2011 Nov;155A(11):2816-20. Epub 2011 Sep 30. PubMed PMID: 219651553.