Craniofacial and extracraniofacial anomalies in craniofacial macrosomia: A multicenter study of 755 patients

被引:52
作者
Caron, Cornelia J. J. M. [1 ]
Pluijmers, Britt I. [1 ]
Wolvius, Eppo B. [1 ]
Looman, Caspar W. N. [2 ]
Bulstrode, Neil [3 ]
Evans, Robert D. [3 ,4 ]
Ayliffe, Peter [4 ]
Mulliken, John B. [5 ]
Dunaway, David [3 ]
Padwa, Bonnie [5 ]
Koudstaal, Maarten J. [1 ,3 ,5 ]
机构
[1] Erasmus MC, Sophias Childrens Hosp, Dept Oral & Maxillofacial Surg, Dutch Craniofacial Ctr, Rotterdam, Netherlands
[2] Erasmus MC, Dept Publ Hlth, Biostat, Rotterdam, Netherlands
[3] Great Ormond St Hosp Sick Children, Craniofacial Unit, London, England
[4] Great Ormond St Hosp Sick Children, Dent & Maxillofacial Surg Dept, London, England
[5] Boston Childrens Hosp, Craniofacial Ctr, Boston, MA USA
关键词
Craniofacial microsomia; Oculo-auriculo-vertebral syndrome; Hemifacial microsomia; OMENS; Retrospective study; Principal component analysis; OMENS-PLUS CLASSIFICATION; HEMIFACIAL MICROSOMIA; OCULOAURICULOVERTEBRAL DYSPLASIA; MORPHOLOGY; VARIANTS; FEATURES;
D O I
10.1016/j.jcms.2017.06.001
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Purpose: Craniofacial microsomia (CFM) is a congenital malformation of structures derived from the first and second pharyngeal arches leading to underdevelopment of the face. However, besides the craniofacial underdevelopment, extracraniofacial anomalies including cardiac, renal and skeletal malformation have been described. The aim of this study is to analyse a large population of patients with regard to demographics, typical phenotypes including craniofacial and extracraniofacial anomalies, and the correlations between the different variables of this condition. Material and methods: A retrospective study was conducted in patients diagnosed with CFM with available clinical and/or radiographic images. All charts were reviewed for information on demographic, radiographic and diagnostic criteria. The presence of cleft lip/palate and extracraniofacial anomalies were noted. Pearson correlation tests and principal component analysis was performed on the phenotypic variables. Results: A total of 755 patients were included. The male-to-female ratio and right-to-left ratio were both 1.2: 1. A correlation was found among Pruzansky-Kaban, orbit and soft tissue. Similar correlations were found between ear and nerve. There was no strong correlation between phenotype and extracraniofacial anomalies. Nevertheless, extracraniofacial anomalies were more frequently seen than in the 'normal' population. Patients with bilateral involvement had a more severe phenotype and a higher incidence of extracraniofacial and cleft lip/palate. Conclusion: Outcomes were similar to those of other smaller cohorts. Structures derived from the first pharyngeal arch and the second pharyngeal arch were correlated with degree of severity. Extracraniofacial anomalies were positively correlated with CFM. The findings show that bilaterally affected patients are more severely affected and should be approached more comprehensively. (C) 2017 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1302 / 1310
页数:9
相关论文
共 35 条
[1]   Role of Environmental Factors in Axial Skeletal Dysmorphogenesis [J].
Alexander, Peter G. ;
Tuan, Rocky S. .
BIRTH DEFECTS RESEARCH PART C-EMBRYO TODAY-REVIEWS, 2010, 90 (02) :118-132
[2]  
[Anonymous], 2002, Principal components analysis
[3]   Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in Europe [J].
Barisic, Ingeborg ;
Odak, Ljubica ;
Loane, Maria ;
Garne, Ester ;
Wellesley, Diana ;
Calzolari, Elisa ;
Dolk, Helen ;
Addor, Marie-Claude ;
Arriola, Larraitz ;
Bergman, Jorieke ;
Bianca, Sebastiano ;
Doray, Berenice ;
Khoshnood, Babak ;
Klungsoyr, Kari ;
McDonnell, Bob ;
Pierini, Anna ;
Rankin, Judith ;
Rissmann, Anke ;
Rounding, Catherine ;
Queisser-Luft, Annette ;
Scarano, Gioacchino ;
Tucker, David .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2014, 22 (08) :1026-1033
[4]   A Phenotypic Assessment Tool for Craniofacial Microsomia [J].
Birgfeld, Craig B. ;
Luquetti, Daniela V. ;
Gougoutas, Alexander J. ;
Bartlett, Scott P. ;
Low, David W. ;
Sie, Kathy C. Y. ;
Evans, Kelly N. ;
Heike, Carrie L. .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2011, 127 (01) :313-320
[5]   HEMIFACIAL MICROSOMIA - FIRST AND SECOND BRANCHIAL ARCH SYNDROME [J].
CONVERSE, JM ;
COCCARO, PJ ;
BECKER, M ;
WOODSMIT.D .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1973, 51 (03) :268-279
[6]  
FRANCOIS J, 1954, Ann Ocul (Paris), V187, P340
[7]  
Goldenhar M., 1952, J GENET HUM, V1, P243
[8]   OCULOAURICULOVERTEBRAL DYSPLASIA [J].
GORLIN, RJ ;
JACOBSEN, U ;
JUE, KL ;
GOLDSCHMIDT, E .
JOURNAL OF PEDIATRICS, 1963, 63 (05) :991-+
[9]  
Grabb W C, 1965, Plast Reconstr Surg, V36, P485, DOI 10.1097/00006534-196511000-00001
[10]  
Heike C.L., 1993, CRANIOFACIAL MICROSO