Introduction: The standard obstetric definition of fetal bradycardia is a sustained fetal heart rate < 110 bpm over at least 10 min. Fetal bradycardia can be the first and only prenatal presentation of a heart disease. We present an overview on different genetic disorders that should be taken into consideration in case of diagnosed fetal bradycardia. Methods: A literature review was conducted using a PubMed- and OMIM-based search for monogenetic disorders causing fetal bradycardia in September 2022. Results: The review on the literature identified nine monogenic diseases that could lead to fetal bradycardia. Four of these disorders can be associated with extracardiac findings. Discussion: Genetic testing should be considered in cases with fetal bradycardia, especially in cases of additional extracardiac findings. Broad sequencing techniques and improved prenatal phenotyping could help to establish a diagnosis in an increasing number of cases.
CITATION STYLE
Westphal, D. S., Hauser, M., Beckmann, B. M., Wolf, C. M., Hessling, G., Oberhoffer-Fritz, R., & Wacker-Gussmann, A. (2022, December 1). Fetal Bradycardia Caused by Monogenic Disorders—A Review of the Literature. Journal of Clinical Medicine. MDPI. https://doi.org/10.3390/jcm11236880
Mendeley helps you to discover research relevant for your work.