Oral and craniofacial manifestations of Ellis-Van Creveld syndrome: a systematic review

被引:16
作者
Lauritano, D. [1 ]
Attuati, S. [1 ]
Besana, M. [1 ]
Rodilosso, G. [1 ]
Quinzi, V [2 ]
Marzo, G. [2 ]
Carinci, F. [3 ]
机构
[1] Univ Milano Bicocca, Neurosci Ctr Milan, Dept Med & Surg, Milan, Italy
[2] Univ Aquila, Post Grad Sch Orthodont, Dept Life Hlth & Environm Sci, Laquila, Italy
[3] Univ Ferrara, Dept Morphol Surg & Expt Med, Ferrara, Italy
关键词
Ellis-Van Creveld syndrome; chondroectodermal dysplasia; dental anomalies; malocclusion; rare diseases; AUTISM SPECTRUM DISORDER; CHILDREN; CILIOPATHIES; MANAGEMENT;
D O I
10.23804/ejpd.2019.20.04.09
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Aim A systematic literature review on oral and craniofacial manifestations of Ellis-Van Creveld syndrome was performed. Methods From 2 databases were selected 74 articles using as key words "Ellis-Van Creveld" AND "Oral" OR "Craniofacial" OR "Dental" OR "Malocclusion". Prisma protocol was used to create an eligible list for the screening. Data were collected in a table to compare the clinical aspects found. Results From the first research emerged 350 articles, and only 72 of them were selected. Conclusion Through this analysis oral and cranio-facial manifestations of Ellis-Van Creveld syndrome were pointed out. Management of Ellis-Van Creveld syndrome requires a multidisciplinary approach involving different clinicians; dentists play an important role in early diagnosis and treatment of the patients.
引用
收藏
页码:306 / 310
页数:5
相关论文
共 43 条
[1]   Oral health problems in leukaemic paediatric patients in the United Arab Emirates: a retrospective study [J].
Alnuaimi, E. ;
Al Halabi, M. ;
Khamis, A. ;
Kowash, M. .
EUROPEAN JOURNAL OF PAEDIATRIC DENTISTRY, 2018, 19 (03) :226-232
[2]  
Aminabadi Naser A, 2010, J Oral Sci, V52, P333
[3]   The Society of Craniofacial Genetics and Developmental Biology 36th Annual Meeting [J].
不详 .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (08) :1873-1875
[4]  
Babaji Prashant, 2010, Indian J Dent Res, V21, P143, DOI 10.4103/0970-9290.62791
[5]   Ellis-van Creveld syndrome with facial hemiatrophy [J].
Bhat, Yasmeen J. ;
Baba, Asif Nazir ;
Manzoor, Sheikh ;
Qayoom, Seema ;
Javed, Sheikh ;
Ajaz, Hakeem .
INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY, 2010, 76 (03) :266-269
[6]   Craniofacial Ciliopathies: A New Classification for Craniofacial Disorders [J].
Brugmann, Samantha A. ;
Cordero, Dwight R. ;
Helms, Jill A. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2010, 152A (12) :2995-3006
[7]   Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium [J].
Caparros-Martin, Jose A. ;
De Luca, Alessandro ;
Cartault, Francois ;
Aglan, Mona ;
Temtamy, Samia ;
Otaify, Ghada A. ;
Mehrez, Mennat ;
Valencia, Maria ;
Vazquez, Laura ;
Alessandri, Jean-Luc ;
Nevado, Julian ;
Rueda-Arenas, Inmaculada ;
Heath, Karen E. ;
Digilio, Maria Cristina ;
Dallapiccola, Bruno ;
Goodship, Judith A. ;
Mill, Pleasantine ;
Lapunzina, Pablo ;
Ruiz-Perez, Victor L. .
HUMAN MOLECULAR GENETICS, 2015, 24 (14) :4126-4137
[8]  
Cesur Y, 2008, EUR J INTERN MED, V5, P187
[9]   Unmasking the ciliopathies: craniofacial defects and the primary cilium [J].
Cortes, Claudio R. ;
Metzis, Vicki ;
Wicking, Carol .
WILEY INTERDISCIPLINARY REVIEWS-DEVELOPMENTAL BIOLOGY, 2015, 4 (06) :637-653
[10]  
Dangulavanich W, 2017, EUR J PAEDIATR DENT, V18, P231, DOI [10.23804/ejpd.201718.03.11, 10.23804/ejpd.2017.18.03.11]