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It includes marked phenotypic variability, even among siblings. Persistent undervirilization despite normal androgen levels should prompt early multidisciplinary evaluation and counseling, especially where genetic testing is limited.<\/jats:p>","DOI":"10.1002\/ccr3.73470","type":"journal-article","created":{"date-parts":[[2026,9,11]],"date-time":"2026-09-11T05:03:04Z","timestamp":1789102984000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["A Likely Diagnosis of Familial Partial Androgen Insensitivity Syndrome in Three 46,\n                    <scp>XY<\/scp>\n                    Siblings With Ambiguous Genitalia: A Case Series"],"prefix":"10.1002","volume":"14","author":[{"ORCID":"https:\/\/orcid.org\/0009-0005-9771-1339","authenticated-orcid":false,"given":"Tayyeb","family":"Ali","sequence":"first","affiliation":[{"name":"Gomal Medical College  Dera Ismail Khan 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