The Committee will meet by webinar on August 30-31, 2022.
Please continue to check this website for the registration link and additional meeting information.
The Advisory Committee on Heritable Disorders in Newborns and Children (Committee) was established under the Public Health Service (PHS) Act, 42 U.S.C. 217a: Advisory councils or committees (PDF - 215 KB), and Title XI § 1111 (42 U.S.C. § 300b-10) (PDF - 209 KB).
The Committee recommends that every newborn screening program include a Uniform Screening Panel (PDF - 12 MB)* that screens for 35 core disorders and 26 secondary disorders; they based the disorders' selection on the Newborn Screening: Towards a Uniform Screening Panel and System (PDF - 191 KB).
The Committee advises the Secretary, U.S. Department of Health and Human Services on the most appropriate application of universal newborn screening tests, technologies, policies, guidelines, and standards. Specifically, the committee provides to the Secretary, the following:
- Advice and recommendations concerning grants and projects authorized awarded or funded related to screening heritable disorders in newborns and children;
- Technical information to develop Heritable Disorders Program policies and priorities will enhance the ability of the state and local health agencies to provide screening, counseling and health care services for newborns and children who have or are at risk for heritable disorders; and
- Recommendations, advice and information to enhance, expand, or improve the ability of the Secretary to reduce mortality and morbidity from heritable disorders in newborns and children.
*Individuals using assistive technology may not be able to fully access information in this file. For assistance, please email HRSAAccessibility@hrsa.gov.