Yıl 2014,
Cilt: 24 Sayı: 4, 230 - 232, 25.09.2014
Öz
Similar to all other system anomalies, congenital nasal anomalies are caused by the defects during embriyogenesis and organogenesis. Nasal tip anomalies are usually accompanied by other systemic pathologies and syndromes. In this article, we report a nose anomaly with the same nasal tip appearance in three siblings.
Anahtar Kelimeler
Kaynakça
- Koç C. Temel Rinoloji. 1. Baskı. Ankara: Güneş Kitabevi; 2009. s. 47-59.
- Losee JE, Kirschner RE, Whitaker LA, Bartlett SP. Congenital nasal anomalies: a classification scheme. Plast Reconstr Surg 2004;113:676-89.
- Patrick R. Carrington, Harold C, James A. Trichorhinophalangeal Syndrome, Type 1. Journal of the American Academy of Dermatology 1994;31:331-6.
- Domingo DL, Freeman AF, Davis J, Puck JM, Tianxia W, Holland SM, et al. Novel intraoral phenotypes in hyperimmunoglobulin-E syndrome. Oral Dis 2008;14:73-81.
- Robinson B, Hilger P. Hereditary agenesis of nasal cartilage. Surgical implications. Arch Otolaryngol Head Neck Surg 1989;115:985-8.
- Innes AM, Chudley AE, Reed MH, Shuckett EP, Hildes- Ripstein GE, Greenberg CR. Third case of cerebral, ocular, dental, auricular, skeletal anomalies (CODAS) syndrome, further delineating a new malformation syndrome: first report of an affected male and review of literature. Am J Med Genet 2001;102:44-7.
- Uçakhan OO, Atmaca L, Sayli BS, Sayar C, Firat E. Bilateral abortive cryptophthalmos associated with oculocutaneous albinism. Acta Ophthalmol Scand 1999;77:238-40.
- Kayserili H, Uz E, Niessen C, Vargel I, Alanay Y, Tuncbilek G, et al. ALX4 dysfunction disrupts craniofacial and epidermal development. Hum Mol Genet 2009;18:4357-66.
Yıl 2014,
Cilt: 24 Sayı: 4, 230 - 232, 25.09.2014
Öz
Doğuştan burun anomalileri, tüm diğer sistem anomalileri gibi embriyogenez ve organogenez sırasındaki hatalardan oluşmaktadır. Nazal tip anomalileri genellikle diğer sistem patolojileri ve sendromlarla birlikte görülür. Bu makalede üç kardeşte aynı nazal tip görünümüne yol açan burun anomalisi sunuldu
Anahtar Kelimeler
Kaynakça
- Koç C. Temel Rinoloji. 1. Baskı. Ankara: Güneş Kitabevi; 2009. s. 47-59.
- Losee JE, Kirschner RE, Whitaker LA, Bartlett SP. Congenital nasal anomalies: a classification scheme. Plast Reconstr Surg 2004;113:676-89.
- Patrick R. Carrington, Harold C, James A. Trichorhinophalangeal Syndrome, Type 1. Journal of the American Academy of Dermatology 1994;31:331-6.
- Domingo DL, Freeman AF, Davis J, Puck JM, Tianxia W, Holland SM, et al. Novel intraoral phenotypes in hyperimmunoglobulin-E syndrome. Oral Dis 2008;14:73-81.
- Robinson B, Hilger P. Hereditary agenesis of nasal cartilage. Surgical implications. Arch Otolaryngol Head Neck Surg 1989;115:985-8.
- Innes AM, Chudley AE, Reed MH, Shuckett EP, Hildes- Ripstein GE, Greenberg CR. Third case of cerebral, ocular, dental, auricular, skeletal anomalies (CODAS) syndrome, further delineating a new malformation syndrome: first report of an affected male and review of literature. Am J Med Genet 2001;102:44-7.
- Uçakhan OO, Atmaca L, Sayli BS, Sayar C, Firat E. Bilateral abortive cryptophthalmos associated with oculocutaneous albinism. Acta Ophthalmol Scand 1999;77:238-40.
- Kayserili H, Uz E, Niessen C, Vargel I, Alanay Y, Tuncbilek G, et al. ALX4 dysfunction disrupts craniofacial and epidermal development. Hum Mol Genet 2009;18:4357-66.
Toplam 8 adet kaynakça vardır.
Ayrıntılar
| Birincil Dil | Türkçe |
|---|---|
| Bölüm | Araştırma Makalesi |
| Yazarlar | |
| Yayımlanma Tarihi | 25 Eylül 2014 |
| Yayımlandığı Sayı | Yıl 2014 Cilt: 24 Sayı: 4 |