{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,24]],"date-time":"2026-09-24T19:40:03Z","timestamp":1790278803941,"version":"4.1.0"},"reference-count":41,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","license":[{"start":{"date-parts":[[2025,5,30]],"date-time":"2025-05-30T00:00:00Z","timestamp":1748563200000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2026,3]]},"abstract":"<jats:p>Prenatal testing has become an increasingly common practice in modern healthcare, offering parents valuable insights into the health and development of their unborn child. However, the rapid advancements in this field have also introduced a host of ethical dilemmas that demand careful consideration. Our objective was to explore the ethical considerations that the clinicians face in prenatal testing and genetic counseling, focusing on issues like informed consent, autonomy, the routinization of testing, disability rights, and implications for practice. A qualitative synthesis of the recent literature published until 2024 was conducted, and the data were organized, recapitulated, and presented to facilitate an integrated, comprehensive approach to prenatal counseling. We concluded that the integration of genetic and genomic testing into routine prenatal care is becoming increasingly common, assisting parents in making informed reproductive decisions. A key ethical concern is ensuring that they are fully informed to make independent choices about testing. Genetic counseling is vital for helping families understand the implications of testing options. However, disparities in access to these services can compromise the informed consent process. We propose a comprehensive approach to prenatal counseling to address these issues.<\/jats:p>","DOI":"10.4103\/ijcm.ijcm_836_24","type":"journal-article","created":{"date-parts":[[2025,5,30]],"date-time":"2025-05-30T08:00:16Z","timestamp":1748592016000},"page":"223-228","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":1,"title":["Assessing the Ethical Considerations in the Era of Advanced Prenatal Testing and Genetic Counselling \u2013 Clinicians\u2019 Perspective"],"prefix":"10.4103","volume":"51","author":[{"given":"Dolat Singh","family":"Shekhawat","sequence":"first","affiliation":[{"name":"Medical Genetics, Department of Pediatrics, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Utkarsha","family":"Kulkarni","sequence":"additional","affiliation":[{"name":"Medical Genetics, Department of Pediatrics, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Charu","family":"Sharma","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pratibha","family":"Singh","sequence":"additional","affiliation":[{"name":"Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kuldeep","family":"Singh","sequence":"additional","affiliation":[{"name":"Medical Genetics, Department of Pediatrics, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2025,5,30]]},"reference":[{"key":"R1-20260416","doi-asserted-by":"crossref","first-page":"298","DOI":"10.3399\/bjgp17X691625","article-title":"Non-invasive prenatal testing: Use of cell-free fetal DNA in Down syndrome screening","volume":"67","author":"Rafi","year":"2017","journal-title":"Br J Gen Pract"},{"key":"R2-20260416","doi-asserted-by":"crossref","first-page":"1589","DOI":"10.1056\/NEJMoa1407349","article-title":"Cell-free DNA analysis for noninvasive examination of trisomy","volume":"372","author":"Norton","year":"2015","journal-title":"N Engl J Med"},{"key":"R3-20260416","doi-asserted-by":"crossref","first-page":"188","DOI":"10.1111\/cga.12481","article-title":"Critical appraisal of droplet digital polymerase chain reaction application for Noninvasive prenatal testing","volume":"62","author":"Shekhawat","year":"2022","journal-title":"Congenit Anom"},{"key":"R4-20260416","doi-asserted-by":"crossref","first-page":"610","DOI":"10.1097\/OGX.0000000000000491","article-title":"What\u2019s new in prenatal genetics? 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