Literature DB >> 18177189

Supernumerary nostril with complete unilateral cleft lip: a case report and review.

Rajesh S Powar1, Vijay R Tubaki.   

Abstract

The supernumerary nostril is an extremely rare congenital anomaly of duplication. A review of the literature shows that only 17 cases have been reported in the world. The supernumerary nostril in association with facial clefting is even more rare, with only three cases reported so far. We are reporting a case of supernumerary nostril in association with complete unilateral cleft lip without cleft palate, which happens to be the first case of its kind to be reported. Most supernumerary nostrils are situated superior to the normal nostrils and very few of them are situated at the same level or below the normal nostrils. In this case, the supernumerary nostril was placed lateral to the normal nostril.

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Year:  2007        PMID: 18177189     DOI: 10.1597/06-115.1

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN: 1055-6656


  2 in total

Review 1.  Supernumerary nostril together with esophageal atresia, imperforate anus and patent ductus arteriosus: a case report and review of the literature.

Authors:  Saeid Aslanabadi; Hamid Djalilian; Sina Zarrintan; Mohammad Sokhandan; Haleh Hashem-Zadeh; Ali Reza Lotfi
Journal:  Pediatr Surg Int       Date:  2009-03-24       Impact factor: 1.827

2.  Nasal Duplication Combined with Cleft Lip and Palate: Surgical Correction and Long-Term Follow-Up.

Authors:  Kanharith Long; Kazuaki Yamaguchi; Daniel Lonic; Vanna Long; Vuthy Chhoeurn; Lun-Jou Lo
Journal:  Plast Reconstr Surg Glob Open       Date:  2017-10-20
  2 in total

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