Congenital Anomalies of the Gastrointestinal Tract Panel

Clinical Use

Use

This test is designed for individuals with clinical or suspected diagnosis of congenital gastrointestinal tract anomalies. It is particularly useful for those presenting with gastrointestinal defects necessitating emergency neonatal surgery or as part of a suspected monogenic or chromosomal syndrome.

Special Instructions

Not provided.

Limitations

While this panel is comprehensive with 180 genes, the performance characteristics have not been cleared or approved by the US Food and Drug Administration. This analysis may not detect all genetic variations related to the congenital anomalies of the gastrointestinal tract.

Test Details

New York Approved