{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,7,30]],"date-time":"2025-07-30T08:07:59Z","timestamp":1753862879467,"version":"3.41.2"},"reference-count":7,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2023,3,15]],"date-time":"2023-03-15T00:00:00Z","timestamp":1678838400000},"content-version":"vor","delay-in-days":14,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Clinical Case Reports"],"published-print":{"date-parts":[[2023,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Congenital hyporhinia, also known as partial arhinia, is a very rare congenital abnormality of nasal embryogenesis with unknown etiology. It is commonly associated with other craniofacial anomalies which are thought to be caused by an absent or rudimentary nose. A 3\u2010h\u2010old neonate presented to our facility with hypoplastic nasal pyramid, hypertelorism, microcephaly, and micrognathia, a case of congenital hyporhinia with associated anomalies is presented and the embryology and literature review are discussed.<\/jats:p>","DOI":"10.1002\/ccr3.7099","type":"journal-article","created":{"date-parts":[[2023,3,16]],"date-time":"2023-03-16T03:48:51Z","timestamp":1678938531000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Congenital hyporhinia with associated malformations: Case report of a rare congenital anomaly"],"prefix":"10.1002","volume":"11","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-9577-5487","authenticated-orcid":false,"given":"Kenneth","family":"Mlay","sequence":"first","affiliation":[{"name":"Kilimanjaro Christian Medical Centre (KCMC)  Moshi Tanzania"},{"name":"Department of Otorhinolaryngology, Head and Neck Surgery Kilimanjaro Christian Medical 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