Upper airway asymmetry in velo-cardio-facial syndrome

被引:36
作者
Chegar, Burke E. [1 ]
Tatum, Sherard A., III [1 ]
Marrinan, Eileen [1 ]
Shprintzen, Robert J. [1 ]
机构
[1] SUNY Upstate Med Univ, Dept Otolaryngol & Commun Sci, Ctr Diag Treatment & Study VeloCardioFacial Syndr, Syracuse, NY 13210 USA
关键词
velo-cardio-facial syndrome; 22q11; deletion; symmetry; pharynx; larynx; nasophary-ngolaryngoscopy; multi-view videofluoroscopy;
D O I
10.1016/j.ijporl.2006.02.007
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: Various forms of asymmetry have been recognized as a feature of velocardio-facial syndrome (VCFS). This study was implemented to determine the frequency of anatomic and functional asymmetry of the velum, pharynx and larynx in children with VCFS. Methods: Individuals with VCFS underwent prospective, blinded analysis by an expert pane[ who assessed the velum, pharynx and larynx with multi-view videofluoroscopy (MVF) and nasopharyngolaryngoscopy (NPL). The VCFS group was compared to an age-matched group of normal individuals. Eight different parameters were assessed in both groups for functional and anatomic symmetry including: velar elevation, adenoid size, posterior pharyngeal wall size, carotid pulsations, epiglottis size and shape, arytenoid size, true vocal cord size and true vocal cord motion. Results: One hundred and twenty-one subjects with VCFS and 20 normal individuals underwent examination. Children with VCFS showed significantly more asymmetry compared to the normal group (69% versus 20%, P = 0.01) with greatest differences seen with palatal motion, posterior pharyngeal wall size and epiglottis shape. On average, subjects with VCFS had three asymmetric parameters versus one parameter in the normal group. Conclusion: Asymmetric development of the pharynx and larynx in children with VCFS appears to be a distinct clinical feature of this syndrome. This finding may provide an important diagnostic clue for patients presenting with subtle features of the 22q11.2 microdeletion. These developmental abnormalities may increase the risk of speech impairment, aspiration and airway obstruction in affected individuals. (C) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1375 / 1381
页数:7
相关论文
共 38 条
[1]  
ARGAMASO RV, 1994, CLEFT PALATE-CRAN J, V31, P287, DOI 10.1597/1545-1569(1994)031<0287:TOAVIW>2.3.CO
[2]  
2
[3]   Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene [J].
Chieffo, C ;
Garvey, N ;
Gong, WL ;
Roe, B ;
Zhang, GZ ;
Silver, L ;
Emanuel, BS ;
Budarf, ML .
GENOMICS, 1997, 43 (03) :267-277
[4]   Pulmonary agenesis: Expansion of the VCFS phenotype [J].
Conway, K ;
Gibson, RL ;
Perkins, J ;
Cunningham, ML .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 113 (01) :89-92
[5]  
D'Antonio LL, 1998, CLEFT PALATE-CRAN J, V35, P333, DOI 10.1597/1545-1569(1998)035<0333:EOPALS>2.3.CO
[6]  
2
[7]  
DANTONIO LL, 1989, CLEFT PALATE J, V26, P217
[8]   Chromosome 22q11.2 deletion and phenotypic features in 30 patients with conotruncal heart defects [J].
Derbent, M ;
Yilmaz, Z ;
Baltaci, V ;
Saygili, A ;
Varan, B ;
Tokel, K .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2003, 116A (02) :129-135
[9]   PREVALENCE OF 22Q11 MICRODELETIONS IN DIGEORGE AND VELOCARDIOFACIAL SYNDROMES - IMPLICATIONS FOR GENETIC-COUNSELING AND PRENATAL-DIAGNOSIS [J].
DRISCOLL, DA ;
SALVIN, J ;
SELLINGER, B ;
BUDARF, ML ;
MCDONALDMCGINN, DM ;
ZACKAI, EH ;
EMANUEL, BS .
JOURNAL OF MEDICAL GENETICS, 1993, 30 (10) :813-817
[10]   Children and adolescents with velocardiofacial syndrome: A volumetric MRI study [J].
Eliez, S ;
Schmitt, JE ;
White, CD ;
Reiss, AL .
AMERICAN JOURNAL OF PSYCHIATRY, 2000, 157 (03) :409-415