Iowa Registry for Congenital and Inherited Disorders
The Iowa Registry for Congenital and Inherited Disorders collects information about infants born with birth defects for the promotion of the health of Iowans by enabling prevention education and connecting families. The University of Iowa, the Department of Human Services and our staff at the Iowa Department of Public Health collaborate on the mission of the registry to:
- Maintain statewide surveillance
- Monitor annual trends
- Conduct research to identify risk factors
- Promote educational activities for the prevention of birth defects
The registry has received national recognition for its role in birth defects surveillance, research and education.
Research produced from the program typically surrounds genetic and environmental risk factors to determine potential causes and treatment protocols for the birth defects including Down syndrome, congenital health defects, neural tube defects and cleft lip and palate. Your participation in these research initiatives is critical to determine potential causes of birth defects. Together, we can pave the way for improved health outcomes for children in Iowa.
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In Iowa, birth defects, neuromuscular disorders, metabolic disorders and stillbirths are reportable conditions. This means that when a baby is born with one of these conditions, it is recorded to the registry.
Birth defects are the leading cause of infant mortality in the United States. About 367 pregnancies per 10,000 are affected each year with a birth defect. A few examples include:
- Congenital heart defects
- Spina bifida
- Cleft lip/cleft palate
- Muscular dystrophy
- Down syndrome
After registered, multiple sources are used to identify infants born with birth defects. Diagnosis, prenatal exposures, prenatal testing and family history trends are all monitored to investigate potential causes.
Confidentiality during this process is incredibly important and rigorously maintained. To learn more about this confidentiality, consult Chapter 22 – Confidential Records.
You and your primary doctor will receive a notification letter and resource information within six months of being identified if your child is placed on the registry as mandated by Iowa Administrative Code. This requirement came about after advocacy from parent groups of children with birth defects.