Congenital Nasal Bones Agenesis: Report of a Rare Malformation

被引:1
作者
Russo, Monica [1 ]
Ferrecchi, Chiara [2 ]
Rebella, Silvia [2 ]
Capra, Valeria [3 ]
Ameli, Franco [4 ]
Pacetti, Mattia [5 ]
Di Feo, Maria Francesca [3 ]
De Biasio, Pierangela [6 ]
Arioni, Cesare [1 ]
机构
[1] IRCCS Osped Policlin San Martino, Operat Unit Neonatol, Genoa, Italy
[2] Univ Genoa, Dept Neurosci Rehabil Ophthalmol Genet Maternal &, Genoa, Italy
[3] IRCCS Ist Giannina Gaslini, Genom & Clin Genet, Genoa, Italy
[4] Casa Cura Villa Montallegro, Otorhinolaringol Dept, Genoa, Italy
[5] IRCCS Ist Giannina Gaslini, Dept Neurosurg, Genoa, Italy
[6] IRCCS Osped Policlin San Martino, Head Fetal Med Unit, Genoa, Italy
关键词
agenesis; arhinia; genetic; hyporhinia; malformation; nasal bones; neonatology; PRENATAL-DIAGNOSIS; TOTAL ARHINIA; DISTRACTION; EXPRESSION; ANOMALIES;
D O I
10.1155/carm/1849957
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Congenital arhinia and hyporhinia are rare facial anomalies whose knowledge usually comes from case reports. The severity of each case described in literature is variable; it also depends on associated malformations too. Since the newborns are obligate nasal breathers, babies with arhinia or hyporhinia usually have respiratory distress and need airway stabilization. In addition, most of these children present difficulties in feeding and this impairment must be managed early. We describe an unusual case of partial congenital arhinia, the baby did not have other anomalies or any specific complication such as respiratory and feeding issues, so the major problem was the aesthetic and psychological issues for the family. Even if the neonatal course was uncomplicated, a coordinated approach of the pediatrician with the pediatric otolaryngologist, the geneticists and the neurosurgeons was necessary because the management of these malformations is always very complex; due to the lack of reports described in literature, an univocal management and also the best timing and technique for reconstructive surgery are still not defined.
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页数:6
相关论文
共 42 条
[1]   Congenital arrhinia: A case report and literature review [J].
Abukhalaf, Sadi A. ;
Zalloum, Jihad S. ;
Al Hammouri, Ahmad ;
Abu Mayaleh, AbdelRazzaq ;
Alzughayyar, Tareq Z. .
INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2020, 135
[2]  
Akkuzu G., 2007, Journal of Medical Case Reports, V1
[3]  
Alansari H, 2018, BAHRAIN MED B, V40, P251
[4]  
Albernaz VS, 1996, AM J NEURORADIOL, V17, P1312
[5]   CRANIOFACIAL ABNORMALITIES INDUCED BY ECTOPIC EXPRESSION OF THE HOMEOBOX GENE HOX-1.1 IN TRANSGENIC MICE [J].
BALLING, R ;
MUTTER, G ;
GRUSS, P ;
KESSEL, M .
CELL, 1989, 58 (02) :337-347
[6]   A Clinical Report of the Complete Nasal Agenesis: Reconstruction of Congenital Arhinia and Review of the Literature [J].
Boynuyogun, Etkin ;
Tuncbilek, Gokhan .
CLEFT PALATE CRANIOFACIAL JOURNAL, 2023, 60 (06) :752-757
[7]   The Role of Maxillary Osteotomy in the Treatment of Arhinia [J].
Brusati, Roberto ;
Colletti, Giacomo .
JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2012, 70 (05) :E361-E368
[8]  
Cohen D., 1987, Rhinology, V25
[9]  
Cohen D., 1986, Rhinology, V24
[10]  
Cong N. V., 2023, Cureus, V15