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We report a term male neonate with bilateral cleft lip and palate, aplasia cutis congenita, postaxial polydactyly, hypotonia, congenital heart disease, and presumed neonatal sepsis. Clinical diagnosis was made without cytogenetic confirmation; the infant died on day five.<\/jats:p>","DOI":"10.1002\/ccr3.73541","type":"journal-article","created":{"date-parts":[[2026,9,16]],"date-time":"2026-09-16T04:58:51Z","timestamp":1789534731000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Recognition of Patau Syndrome (Trisomy 13) Based on Clinical Features in a Resource\u2010Limited Setting: A Case Report"],"prefix":"10.1002","volume":"14","author":[{"ORCID":"https:\/\/orcid.org\/0009-0001-3595-5531","authenticated-orcid":false,"given":"Sayed Hussain","family":"Amiri","sequence":"first","affiliation":[{"name":"Department of Paraclinic, Faculty of Curative Medicine Shifa University  Kabul Afghanistan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nasir Ahmad","family":"Anwari","sequence":"additional","affiliation":[{"name":"Department of Pediatric Medicine Atat\u00fcrk Children's 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