Genomic Sequencing for the Evaluation of Fetal Structural Anomalies

Principal Investigator: Mary Norton, MD

The purpose of this study is to assess the effectiveness of sequencing as a tool for diagnosing the underlying genetic cause in fetuses with structural anomalies and to help define prenatal presentation of genetic diseases. Identification of a genetic diagnosis may help providers predict outcomes and counsel patients in the prenatal and postnatal periods.

Research Coordinator:

Katie Tick       

Uncovering the Etiologies of Non-immune hydrops fetalis Through Comprehensive Genomic Analyses and Phenotyping

Principal Investigator: Teresa Sparks, MD, MAS

The purpose of this multi-site study is to better understand the genetic causes of non-immune hydrops fetalis (NIHF) via genomic sequencing. Determining the various underlying causes of NIHF can help providers take a more precision-based approach in the care of affected pregnancies and newborns, as well as in counseling patients regarding future pregnancies.

Research Coordinator:

Katie Tick

To learn more about study participation, email ​[email protected] or click navy blue button on the right.