Bill

Bill > A1988


NJ A1988

NJ A1988
Establishes central registry for sickle cell trait diagnoses; provides for informational outreach and genetic counseling.


summary

Introduced
01/11/2022
In Committee
02/28/2023
Crossed Over
02/27/2023
Passed
Dead
01/08/2024

Introduced Session

2022-2023 Regular Session

Bill Summary

Establishes central registry for sickle cell trait diagnoses; provides for informational outreach and genetic counseling.

AI Summary

This bill establishes a central registry for sickle cell trait diagnoses in New Jersey. It requires laboratories performing newborn screenings to notify the patient's physician and document the diagnosis in the registry. The physician must then provide the patient's parents with information about the availability and benefits of genetic counseling. The bill also requires the Commissioner of Health to establish a system to notify patients and their parents about follow-up consultations and educational services related to sickle cell trait. The information in the registry will be kept confidential, except as provided by law, and disclosing information in violation of this provision is a disorderly persons offense.

Committee Categories

Health and Social Services

Sponsors (10)

Last Action

Received in the Senate, Referred to Senate Health, Human Services and Senior Citizens Committee (on 02/28/2023)

bill text


bill summary

Loading...

bill summary

Loading...
Loading...