| Literature DB >> 7732122 |
G S LaTrenta1, H W Choi, R F Ward, L Hoffman, J A Neidich.
Abstract
Complete nasal aplasia is an extremely rare clinical entity and most infants are stillborn when this is associated with holoprosencephaly. A viable 3-year-old infant born with frontonasal arrest without holoprosencephaly is presented. The child's main complaint was lack of a nasal airway, which made eating extremely difficult. A method for craniofacial reconstruction of the nasopharynx is presented.Entities:
Mesh：
Year: 1995 PMID： 7732122 DOI： 10.1097/00006534-199505000-00024
Source DB: PubMed Journal: Plast Reconstr Surg ISSN： 0032-1052 Impact factor: 4.730