S 3322
Establishes central registry for sickle cell trait diagnoses; provides for informational outreach and genetic counseling.
Take action
Record your position on this measure.
Sign in to record your position, submit testimony, or contact your legislator.
Sign in to take action- Introduced
- Passed Senate
- Passed General Assembly
- To Governor
- Became Law
Bill overview
This bill creates a central registry in New Jersey to track newborns diagnosed with sickle cell trait. It requires laboratories to notify physicians and parents about the diagnosis and makes available genetic counseling information. The registry will be used to gather data and provide ongoing support and education to patients and their families, including periodic notifications about potential health implications and available resources.
Arguments in favor
Reasons to support this legislation.
No arguments in favor have been submitted.
Submit yoursArguments opposed
Reasons to oppose this legislation.
No arguments opposed have been submitted.
Submit yoursRead the latest version inline or switch to a previous version.