Supernumerary nostril: Congenital adrenal hyperplasia with a rare congenital anomaly

Multiple or supernumerary nostril is a rare congenital anomaly with unknown etiology. The first case was reported by Lindsay as bilateral supernumerary nostrils. Supernumerary nostril cases are mostly unilateral and isolated. They are also reported with other congenital malformations like facial cle...

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Autores principales: Ciloglu, Sinem, Duran, Alpay, Buyukdogan, Hasan, Yigit, Ahmet K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Case Report - Developmental Anomalies
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4293843/
https://www.ncbi.nlm.nih.gov/pubmed/25593872
http://dx.doi.org/10.4103/2231-0746.147133
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author Ciloglu, Sinem
Duran, Alpay
Buyukdogan, Hasan
Yigit, Ahmet K.
author_facet Ciloglu, Sinem
Duran, Alpay
Buyukdogan, Hasan
Yigit, Ahmet K.
author_sort Ciloglu, Sinem
collection PubMed
description Multiple or supernumerary nostril is a rare congenital anomaly with unknown etiology. The first case was reported by Lindsay as bilateral supernumerary nostrils. Supernumerary nostril cases are mostly unilateral and isolated. They are also reported with other congenital malformations like facial clefts and congenital anomalies like congenital auricular hypoplasia, congenital cataracts, eusophageal atresia and patent ductus arteriosus. Here, we report a case of supernumerary nostril with congenital adrenal hyperplasia
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spelling pubmed-42938432015-01-15 Supernumerary nostril: Congenital adrenal hyperplasia with a rare congenital anomaly Ciloglu, Sinem Duran, Alpay Buyukdogan, Hasan Yigit, Ahmet K. Ann Maxillofac Surg Case Report - Developmental Anomalies Multiple or supernumerary nostril is a rare congenital anomaly with unknown etiology. The first case was reported by Lindsay as bilateral supernumerary nostrils. Supernumerary nostril cases are mostly unilateral and isolated. They are also reported with other congenital malformations like facial clefts and congenital anomalies like congenital auricular hypoplasia, congenital cataracts, eusophageal atresia and patent ductus arteriosus. Here, we report a case of supernumerary nostril with congenital adrenal hyperplasia Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4293843/ /pubmed/25593872 http://dx.doi.org/10.4103/2231-0746.147133 Text en Copyright: © Annals of Maxillofacial Surgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report - Developmental Anomalies
Ciloglu, Sinem
Duran, Alpay
Buyukdogan, Hasan
Yigit, Ahmet K.
Supernumerary nostril: Congenital adrenal hyperplasia with a rare congenital anomaly
title Supernumerary nostril: Congenital adrenal hyperplasia with a rare congenital anomaly
title_full Supernumerary nostril: Congenital adrenal hyperplasia with a rare congenital anomaly
title_fullStr Supernumerary nostril: Congenital adrenal hyperplasia with a rare congenital anomaly
title_full_unstemmed Supernumerary nostril: Congenital adrenal hyperplasia with a rare congenital anomaly
title_short Supernumerary nostril: Congenital adrenal hyperplasia with a rare congenital anomaly
title_sort supernumerary nostril: congenital adrenal hyperplasia with a rare congenital anomaly
topic Case Report - Developmental Anomalies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4293843/
https://www.ncbi.nlm.nih.gov/pubmed/25593872
http://dx.doi.org/10.4103/2231-0746.147133
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AT buyukdoganhasan supernumerarynostrilcongenitaladrenalhyperplasiawithararecongenitalanomaly
AT yigitahmetk supernumerarynostrilcongenitaladrenalhyperplasiawithararecongenitalanomaly

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