Nasal fossa malformations and paramedian facial cleft: New perspectives

Citation
En. Garabedian et al., Nasal fossa malformations and paramedian facial cleft: New perspectives, J CRAN GENE, 19(1), 1999, pp. 12-19
Citations number
23
Categorie Soggetti
Molecular Biology & Genetics
Journal title
JOURNAL OF CRANIOFACIAL GENETICS AND DEVELOPMENTAL BIOLOGY
ISSN journal
02704145 → ACNP
Volume
19
Issue
1
Year of publication
1999
Pages
12 - 19
Database
ISI
SICI code
0270-4145(199901/03)19:1<12:NFMAPF>2.0.ZU;2-L
Abstract
Choanal atresia may be associated with other cranio-facial malformations, i ncluding various degrees of nasal fossa malformation, and may be a part of paramedian facial clefts (as described by Tessier et al. [1977]). We identi fied five such cases with combined clinical elements corresponding to Tessi er's paramedian facial cleft, including eyelid coloboma, mild to severe cho anal and nasal fossa anomalies, ethmoidal hypoplasia and anterior skull bas e malformation, sometimes with proboscis lateralis and half-nose hypoplasia . These observations incited us, first, to elaborate a conception which accou nts for the likely embryological mechanisms involved; second, to propose a new classification based on anatomical and pathogenic embryological conside rations; and last, to propose the use of transpalatal approach to restore c hoanal permeability, since endonasal laser therapy is particularly dangerou s in such cases.