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                  <mods:namePart>Cid-Galache, P</mods:namePart>
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                  <mods:namePart>Casas-Gómez, J</mods:namePart>
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                  <mods:namePart>Broncano-Lupiáñez, S</mods:namePart>
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                  <mods:namePart>Rodríguez-Leal, A</mods:namePart>
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               <mods:identifier type="citation">Boletín del ECEMC: Rev Dismor Epidemiol 2010; V (nº 9): 15-19</mods:identifier>
               <mods:identifier type="issn">0210–3893</mods:identifier>
               <mods:identifier type="journal">Boletín del ECEMC: Revista de Dismorfología y Epidemiología</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/14072</mods:identifier>
               <mods:abstract>Supernumerary or accessory nostrils are a very rare type of congenital nasal anomaly, with only a few cases reported in the literature. They can be associated with other malformations such as cleft palate and they can be unilateral or bilateral, with most cases reported being unilateral. The accessory nostril may or may not communicate with the ipsilateral nasal cavity, probably depending on the degree of embryological progression of the anomaly. A case of double supernumerary nostril with no nasal cavity communication and with an otherwise normally developed nose is presented. The surgical treatment is described and the different speculative theories related to the embryogenesis of supernumerary nostrils are also reviewed.</mods:abstract>
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                  <mods:title>Fosa nasal supernumeraria, una extraña malformación congénita. Primer caso registrado por el ECEMC</mods:title>
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