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history.<\/jats:p><\/jats:list-item>\n<\/jats:list>\n<\/jats:p><jats:p><jats:bold>What does this study add?<\/jats:bold>\n<jats:list list-type=\"bullet\">\n<jats:list-item><jats:p>This case underscores the limitations of NIPS for monogenic conditions in low\u2010risk populations and the importance of pre\u2010 and post\u2010test genetic counseling, family history, and parental testing.<\/jats:p><\/jats:list-item>\n<jats:list-item><jats:p>Further research is needed to determine the clinical utility of NIPS for single gene disorders in low\u2010risk populations.<\/jats:p><\/jats:list-item>\n<\/jats:list>\n<\/jats:p>","DOI":"10.1002\/pd.6549","type":"journal-article","created":{"date-parts":[[2024,3,9]],"date-time":"2024-03-09T07:18:29Z","timestamp":1709968709000},"page":"398-400","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Caution with noninvasive prenatal screening for single gene disorders: A case report of a 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