Addressing the Burdens That Newborn Screening Imposes on Underserved Communities

Meghan E Strenk¹, Courtney Berrios^{2

3}, Jeremy R Garrett^{1

3}

Affiliations

Comment

Meghan E Strenk et al. Am J Bioeth. 2023 Jul.

. 2023 Jul;23(7):79-82.

doi: 10.1080/15265161.2023.2207542.

Meghan E Strenk¹, Courtney Berrios^{2

3}, Jeremy R Garrett^{1

3}

No abstract available

Comment on

Rare Disease, Advocacy and Justice: Intersecting Disparities in Research and Clinical Care.
Halley MC, Halverson CME, Tabor HK, Goldenberg AJ. Halley MC, et al. Am J Bioeth. 2023 Jul;23(7):17-26. doi: 10.1080/15265161.2023.2207500. Epub 2023 May 19. Am J Bioeth. 2023. PMID: 37204146 Free PMC article.

1. Aronovich Elena L., Pan Dao, and Whitley Chester B.. “Molecular genetic defect underlying alpha-L-iduronidase pseudodeficiency.” American journal of human genetics 58, no. 1 (1996): 75. - PMC - PubMed
1. Tajima Youichi, Matsuzawa Fumiko, Aikawa Sei-ichi, Okumiya Toshika, Yoshimizu Michiru, Tsukimura Takahiro, Ikekita Masahiko et al. “Structural and biochemical studies on Pompe disease and a “pseudodeficiency of acid α-glucosidase”.” Journal of human genetics 52 (2007): 898–906. - PubMed
1. Pollard L, Braddock SR, Christensen KM, Boylan DJ, Smith LD, A Heese B, M Atherton A, Lawson CE, Strenk ME, Willing M, Manwaring L, Wood TC. “Inborn errors of metabolism: from identification to treatment.” (Abstract 82, presentation at the American Society of Human Genetics 63rd Annual Meeting, Boston, MA: October 23, 2013.
1. Strenk M, N Gadea R, Heese BA, Gannon JL. “Newborn screening for four Lysosomal Storage Disorders: One center’s experience over six years.” (Poster, presented at the National Society of Genetic Counselors 38th Annual Education Conference, Salt Lake City, UT, November 5–8, 2019
1. “Recommended Uniform Screening Panel.” HRSA. Health Resources and Services Administration, March 30, 2023. https://www.hrsa.gov/advisory-committees/heritable-disorders/rusp.