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DMD is a multi\u2010system disease resulting in muscle weakness with progressive deterioration of skeletal, heart, and smooth muscle, and learning disabilities. Pathogenic\/likely pathogenic (P\/LP) variants in the <jats:italic>DMD<\/jats:italic> gene, which encodes dystrophin protein, cause dystrophinopathy. All males with a P\/LP variant in the X\u2010linked <jats:italic>DMD<\/jats:italic> gene are expected to be affected. Two to 20% of female heterozygotes with a P\/LP variant develop symptoms of dystrophinopathy ranging from mild muscle weakness to significant disability similar to Becker muscular dystrophy. Recently, with improvements in therapies and testing methodology, there is stronger evidence supporting newborn screening (NBS) for DMD for males and females because females may also develop symptoms. A consented pilot study to screen newborns for DMD was initiated in New York State (NYS) and conducted from 2019 to 2021. The identification of female carriers and the realization of the subsequent uncertainty of providers concerning follow\u2010up during the pilot led to the development of algorithms for screening and diagnosis of carrier females, including both NBS and cascade molecular testing of family members.<\/jats:p>","DOI":"10.1002\/ajmg.c.32000","type":"journal-article","created":{"date-parts":[[2022,9,24]],"date-time":"2022-09-24T18:43:35Z","timestamp":1664045015000},"page":"197-205","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":23,"title":["Newborn screening for Duchenne muscular dystrophy\u2010early detection and diagnostic algorithm for female carriers of Duchenne muscular dystrophy"],"prefix":"10.1002","volume":"190","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-5806-0127","authenticated-orcid":false,"given":"Dorota","family":"Gruber","sequence":"first","affiliation":[{"name":"Department of Pediatrics Cohen Children's 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