Description
Seeking infants admitted to the NICU with an unexplained likely genomic illness for a study of the benefit of genomic testing on their care.
Overview
Participants in this study will have genomic sequencing for 73 genes known to cause medical issues completed on both the newborn and one of their parents.
What we're hoping for
We are studying hot to improve medical practice and patient care for newborns who have an unexplained, but likely genetic illness.
Additional Information
ClinicalTrials.gov Identifier: NCT05205356