Unusual nasal duplication in two patients

Guion‐Almeida, Maria Leine; Neto, Domingos Lamônica; Lopes, Vera Lúcia Gil da Silva

doi:10.1002/ajmg.a.30278

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Cited by 7 publications

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“…A supernumerary nostril may or may not communicate with the ipsilateral normal nasal cavity, depending on the extent of the anomaly's progression [19] . This condition should not be confused with the double nose deformity which has 2 septums, 4 nostrils, 4 alaes and 4 cavities [20] .…”

Section: Discussionmentioning

confidence: 99%

Supernumerary Nostril

Sun

H²,

Zhang³

et al. 2009

Eur Surg Res

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Section: Discussionmentioning

confidence: 99%

Supernumerary Nostril

Sun

H²,

Zhang³

et al. 2009

Eur Surg Res

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Supernumerary nostril together with esophageal atresia, imperforate anus and patent ductus arteriosus: a case report and review of the literature

et al. 2009

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Supernumerary nostril is an extremely rare congenital entity which results from aberrant embryological development. The review of the literature reveals that only 30 cases of supernumerary nostril have been reported. We report a rare case of supernumerary nostril in association with esophageal atresia, imperforate anus, and patent ductus arteriosus. To our knowledge, this is the first case of supernumerary nostril which has been accompanied by three other congenital anomalies. In addition to the presented case, we review all the literature cases of supernumerary nostril.

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