Congenital arhinia

Journal of Paediatrics and Child Health

Volumn 39, Issue 6, 2003, Pages 474-476

  McGlone, L ^a,b  

^a QUEEN MOTHER S HOSPITAL   (United Kingdom)

^b Princess Royal Maternity Hospital ^*  (United Kingdom)

Author keywords

Arhinia; Congenital; Neonate

Indexed keywords

ELECTROLYTE; GONADOTROPIN; HYDROCORTISONE; LUTEINIZING HORMONE; THYROTROPIN;

ARTICLE; ARTIFICIAL VENTILATION; CASE REPORT; CHROMOSOME ANALYSIS; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL ARHINIA; CONGENITAL MALFORMATION; FACE MALFORMATION; FUNCTION TEST; HUMAN; MALE; MICROPENIS; NEWBORN; NOSE RECONSTRUCTION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRENATAL PERIOD; PRIORITY JOURNAL; RESPIRATORY DISTRESS; TRACHEOSTOMY;

HUMANS; INFANT, NEWBORN; MALE; NOSE;

EID: 0141613873     PISSN: 10344810     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1440-1754.2003.00193.x     Document Type: Article

References (25)

1. Blair VP, Brown JB. Nasal abnormalities, fancied and real. Surg. Gynecol. Obstet. 1931; 53: 796-819.
2. Palmer CR, Thomson HG. Congenital absence of the nose: a case report. Can. J. Surg. 1967; 10: 83-6.
3. Berger M, Martin C. Total arhinogenesis apropos of an unusual case. Rev. Laryngol. Otol. Rhinol. 1969; 90: 300-19.
4. Gifford Jr GH, Swanson L, MacCollum DW. Congenital absence of the nose and anterior nasopharynx. Report of two cases. Plast. Reconstr. Surg. 1972; 50: 5-12.
5. Kemble JV. The importance of the nasal septum in facial development. J. Laryngol. Otol. 1973; 87: 379-86.
6. Lutolf U. Bilateral aplasia of the nose: a case report. J. Maxillofac. Surg. 1976; 4: 245-9.
7. Ruprecht KW, Majewski F. Familial arhinia combined with Peters' anomaly and maxiliary deformities, a new malformation syndrome. Klin. Monatsbl. Augenheilkd. 1978; 172: 708-15.
8. Das Gupta HK, Gupta V, Gupta M. Absent nose. Br. J. Plast. Surg. 1979; 32: 85-6.
9. Shubich I, Sanchez C. Nasal aplasia associated with meningocele and submucous cleft palate. Ear Nose Throat J. 1985; 64: 259-60.
10. Kaminker CP, Dain L, Lamas MA et al. Mosaic trisomy 9 syndrome with unusual phenotype. Am. J. Med. Genet. 1985; 2: 237-41.
11. Cohen D, Goitein KJ. Arhinia. Rhinology 1986; 24: 287-92.
12. Cohen D, Goitein KJ. Arhinia revisited. Rhinology 1987; 25: 237-44.
13. Cole RR, Myer CM, Bratcher GO. Congenital absence of the nose: a case report. Int. J. Pediatr. Otorhinolaryngol. 1989; 17: 171-7.
14. Navarro-Villa C, Matias GC, Martinez GC et al. Congenital absence of the nose and nasal fossae. J. Cranio-Maxillofac. Surg. 1991; 19: 56-60.
15. Weinberg A, Neuman A, Benmeir P et al. A rare case of arhinia with severe airway obstruction: case report and review of the literature. Plast. Reconst. Surg. 1993; 91: 146-9.
16. Muhlbauer W, Schmidt A, Fairley J. Simultaneous construction of an internal and external nose in an infant with arhinia. Plast. Reconstr. Surg. 1993; 91: 720-5.
17. Galleti R, Dallari S, Bruzzi M et al. Considerations concerning respiratory physiopathology in a case of total arhinia. Acta Otorhinolaryngol. Ital. 1994; 4: 63-9.
18. LaTrenta GS, Choi HW, Ward RF et al. Complete nasal agenesis with bilateral microphthalmia and unilateral duplication of the thumb. Plast. Reconstr. Surg. 1995; 95: 1101-4.
19. Albernaz VS, Castillo M, Mukherji SK et al. Congenital arhinia. AJNR 1996; 17: 1312-14.
20. Thiele H, Musil A, Nagel F et al. Familial arhinia, choanal atresia and microphthalmia. Am. J. Med. Genet. 1996; 63: 310-13.
21. Hansen M, Lucarelli MJ, Whiteman DA et al. Treacher-Collins syndrome: phenotypic variability in a family including an infant with arhinia and uveal colobomas. Am. J. Med. Genet. 1996; 61: 71-4.
22. Meyer R. Total external and internal construction in arhinia. Plast. Reconstr. Surg. 1997; 99: 534-42.
23. Cusick W, Sullivan CA, Rojas B et al. Prenatal diagnosis of total arhinia. Ultrasound Obstet. Gynaecol. 2000; 15: 259-61.
24. Olsen OE, Gjelland K, Reigstad H et al. Congenital absence of the nose: a case report and literature review. Pediatr. Radiol. 2001; 31: 225-32.
25. Nishimura Y. Embryological study of nasal cavity development in human embryos with reference to congenital nostril atresia. Acta Anat. 1993; 147: 140-4.