Drazba, Katy

Lead Genetic Counselor

Drazba, Katy

Katy joined the Greenwood Genetic Center in 2016. She is a graduate of the Genetic Counseling Training Program at the University of Alabama at Birmingham. Katy currently provides genetic counseling services for the Columbia office. She is a member of the National Society of Genetic Counselors and is certified by the American Board of Genetic Counseling.

Contact Information

Office (803) 391-3812
Fax (803) 799-5391
kdrazba@ggc.org

Education and Related Experience

  • B.S., Biology, Loyola Marymount University, Los Angeles, CA, 2006
  • M.P.H., Maternal & Child Health, University of Illinois at Chicago, 2010
  • Research Assistant, LSU Pennington Biomedical Research Center, Baton Rouge, LA, 2010-14
  • M.S., Genetic Counseling, University of Alabama Birmingham, 2016

Publications

  • Bell S, Butler KM, Drazba KT, Lynch J, Abidi FE, DuPont B, Stevenson RE. (2022). Angelman syndrome with a 15q11q13 deletion in a mother and daughter. Clinical Dysmorphology, 31(2), 91-93. doi: 10.1097/MCD.0000000000000399. https://pubmed.ncbi.nlm.nih.gov/34775449/
  • Drazba KT, Denton JJ, Barger Hurst C, McGwin G, MacLennan PA, Ovalle F. (2021). Incorporation of a genetics-based information module into standardized diabetes patient education. Primary Care Diabetes, 15(4), 706-712. doi: 10.1016/j.pcd.2021.04.013. https://pubmed.ncbi.nlm.nih.gov/33994279/ 
  • Hollenbeck D, Williams CL, Drazba K, Descartes M, Korf BR, Rutledge SL, Lose EJ, Robin NH, Carroll AJ, Mikhail FM. (2017). Clinical relevance of small copy-number variants in chromosomal microarray clinical testing. Genetics in Medicine, 19(4), 377-385. doi: 10.1038/gim.2016.132. https://www.ncbi.nlm.nih.gov/pubmed/27632688
  • Drazba KT, Kelley MA, Hershberger PE. (2014). A Qualitative Inquiry of the Financial Concerns of Couples Opting to Use Preimplantation Genetic Diagnosis to Prevent the Transmission of Known Genetic Disorders. Journal of Genetic Counseling, 23(2), 202-211. doi: 10.1007/s10897-013-9638-7. https://www.ncbi.nlm.nih.gov/pubmed/23949612

Meet the Shenal Family

Our daughter, Ryleigh, was diagnosed with a rare chromosomal deletion shortly after she was born in 2010. Since we received her diagnosis, the Greenwood Genetic Center has become part of our family. They made certain that we did not feel alone, and they continue to provide ongoing, compassionate care for our child. The impact they have had on our family and others across the globe everyday is immeasurable. We can't imagine walking this journey without...

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