Kestutis Micke, MS, CGC
Sr. Instructor, OB-GYN-Maternal Fetal Medicine
Graduate School
- MS, University of Michigan (2018)
Undergraduate School
- BS, University of Minnesota–Twin Cities (MN) (2013)
Languages
EnglishDepartment
OB-GYN-Maternal Fetal MedicineProfessional Titles
- Genetic Counselor
Publications
- Christopher D, Fringuello M, Fought AJ, Bolt M, Micke K, Elfman H, Reeves S. Evaluating for disparities in prenatal genetic counseling. Am J Obstet Gynecol MFM. 2021 Sep 25;4(1):100494. [Epub ahead of print] PubMed PMID: 34583054
- Micke, Kestutis, et al. "Megacystis associated with an underlying ACTA2 variant and diagnosis of multisystemic smooth muscle dysfunction syndrome: A case report." Urology (2022).
- Micke, K. C., Elfman, H. M., Fantauzzo, K. A., McGrath, P. S., Clouthier, D. E., McCandless, S. E., ... & Zaretsky, M. V. (2023). Piloting a multidisciplinary approach to improve outcomes of fetal whole exome sequencing: An overview of workflow and case example. Prenatal Diagnosis.
- Crenshaw, M. M., Thompson, L., Piqué, D. G., Micke, K., Saenz, M., & Baker, P. R. (2023). Congenital diaphragmatic hernia in siblings with PIGA-related congenital disorder of glycosylation. American Journal of Medical Genetics Part A
- Putra, M., Lee, Y.M., Bucholz, E., Ross, E., Galan, H., Behrendt, N., Micke, K., Chow, F., Zaretsky, M., Cuneo, B. (2023). Successful Management of Fetal Torsades de Pointes and Long QT Syndrome by a Cardio-Obstetrical Team. Journal of American College of Cardiologists: Case Reports.
- Walsh CJ, Micke K, Elfman H, Bock M, Harper T, Zaretsky M, Galan HL, Behrendt N, Putra M. Successful antenatal treatment of MAGED2-related Bartter syndrome and review of treatment options and efficacy. Prenat Diagn. 2024 Feb;44(2):172-179. PubMed PMID: 38159268
- Putra M, Lee YM, Bucholz E, Ross EL, Galan H, Behrendt N, Micke K, Chow FS, Zaretsky MV, Cuneo BF. Successful Management of Fetal Torsades de Pointes and Long QT Syndrome by a Cardio-Obstetrical Team. JACC Case Rep. 2023 Dec 6;27:102110. PubMed PMID: 38094730
- Crenshaw MM, Thompson L, Piqué DG, Micke K, Saenz M, Baker PR 2nd. Congenital diaphragmatic hernia in siblings with PIGA-related congenital disorder of glycosylation. Am J Med Genet A. 2023 Dec;191(12):2860-2867. PubMed PMID: 37589195
Professional Memberships
- National Society of Genetic Counselors, Member
Practice Locations
Children's Hospital Colorado - Colorado Fetal Care Center13123 E 16th Ave, B735
Aurora, CO 80045
720-777-4463
Hospital Affiliation
- University of Colorado Hospital
- Children's Hospital Colorado
Center Affiliations
Specialty Information
Specialties- Obstetrics and Gynecology, Board Certification
- American Board of Genetic Counseling, Board Certification (0001)
- Pregnancy and Reproduction - Prenatal Testing
- Pregnancy and Reproduction
- Genetic Conditions and Testing
Clinical Interests
My clinical interests include working with families to prenatally diagnose genetic syndromes. I am particularly interested in helping families whose pregnancy has been found to have fetal anomalies. Depending on the constellation of anomalies present, I inform families regarding what diagnoses may be most likely, as well as the genetic testing options that are available to them. I interpret genetic testing results for families to understand the impact of the genetic findings. I frequently come across rare chromosomal abnormalities and have embraced whole exome sequencing, which is a new genetic testing technology in the prenatal setting.
Care Philosophy
I believe that an educated patient is an empowered patient. Empowered patients make decisions that are aligned with their lifestyle and values, ultimately resulting in the best outcomes for their families. I strive to ensure that patients understand genetic information and its implications, so they can make decisions regarding their pregnancy.
My clinical interests include working with families to prenatally diagnose genetic syndromes. I am particularly interested in helping families whose pregnancy has been found to have fetal anomalies. Depending on the constellation of anomalies present, I inform families regarding what diagnoses may be most likely, as well as the genetic testing options that are available to them. I interpret genetic testing results for families to understand the impact of the genetic findings. I frequently come across rare chromosomal abnormalities and have embraced whole exome sequencing, which is a new genetic testing technology in the prenatal setting.
Care Philosophy
I believe that an educated patient is an empowered patient. Empowered patients make decisions that are aligned with their lifestyle and values, ultimately resulting in the best outcomes for their families. I strive to ensure that patients understand genetic information and its implications, so they can make decisions regarding their pregnancy.