Congenital Complete Arhinia: Report of a Rare Case.

dc.contributor.authorBiswas, Kaustuv Das
dc.contributor.authorDutta, Kaustuv Das
dc.contributor.authorGhatak, Soumya
dc.contributor.authorSinha, Ramanuj
dc.date.accessioned2015-07-09T04:09:05Z
dc.date.available2015-07-09T04:09:05Z
dc.date.issued2014-11
dc.description.abstractCongenital absence of the nose (arhinia) is extremely rare. Arhinia leads to severe airway impairment and poor feeding in the neonate. Th e degree of nasal absence varies from case to case. Here, we present a case of congenital complete arhinia associated with other craniofacial anomalies. Arhinia leads to severe respiratory distress and feeding problems in newborn warranting emergency management, but our case diff ers as the child was adapted to mouth breathing and naso-gastric tube feeding, giving us the opportunity to delay the defi nitive management for a few weeks yet avoiding the risk of operating in a small child to create nasal airway or tracheostomy on an emergency basis.en_US
dc.identifier.citationBiswas Kaustuv Das, Dutta Kaustuv Das, Ghatak Soumya, Sinha Ramanuj. Congenital Complete Arhinia: Report of a Rare Case. IJSS Case Reports & Reviews. 2014 Nov; 1(6): 8-10.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/159348
dc.language.isoenen_US
dc.source.urihttps://www.ijsscr.com/sites/default/files/articles/IJSS-1-8_1.xmlen_US
dc.subjectArhiniaen_US
dc.subjectCongenital anomaliesen_US
dc.subjectNewbornen_US
dc.subject.meshChoanal Atresia --diagnosis
dc.subject.meshChoanal Atresia --therapy
dc.subject.meshCongenital Abnormalities --epidemiology
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshInfant, Newborn
dc.subject.meshMicrophthalmos --diagnosis
dc.subject.meshMicrophthalmos --therapy
dc.subject.meshNose --abnormalities
dc.subject.meshPremature Birth
dc.titleCongenital Complete Arhinia: Report of a Rare Case.en_US
dc.typeArticleen_US
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