Published Aug 24, 2020



PLUMX
Almetrics
 
Dimensions
 

Google Scholar
 
Search GoogleScholar


Aura Alejandra Viteri Rentería https://orcid.org/0000-0002-7322-6129

Ana del Carmen Armas Vega https://orcid.org/0000-0003-3800-8166

Álex Esteban Carrera Robalino https://orcid.org/0000-0003-1049-7930

Adriana Patricia Paltas Miranda https://orcid.org/0000-0003-3705-8778

Mayra Elizabeth Paltas Miranda https://orcid.org/0000-0003-3441-6015

##plugins.themes.bootstrap3.article.details##

Abstract

Background: Cri du Chat syndrome (SCdC) is a low-prevalence genetic disorder. It is important that clinical dentists know about its craniofacial and stomatological characteristics, as well as considerations for an adequate treatment of these patients. Purpose: to identify recent advances in the diagnosis and treatment of patients with SCdC. Methods: in this systematic review, PubMed, SciELO, LiLACS, and TripDatabase were searched. Search terms were “Cri du Chat” and “cat howl syndrome and dentistry,” between 2003 and 2018. 25 articles that met the inclusion and exclusion criteria were obtained and analyzed. Results: the low frequency of appearance of the syndrome was confirmed. Representative craniofacial and oral characteristics associated with micrognathism and retrognathism that alter the patient's facial appearance were identified. Alterations such as dental crowding, malocclusion, and associated periodontal disease can be corrected and controlled with adequate oral hygiene and nutritional guidance for the patient and their parents. Conclusions: SCdC is rare. Its pathognomonic characteristics appear in childhood and adolescence, so they require more attention. Early detection makes it possible to propose an adequate treatment to improve the patients’ quality of life.

Keywords

cat cry syndrome, child, Cri-du-Chat syndrome, dentistry, dentists, diagnostics, oral medicine, oral pathology, oral semiology, pediatric dentistry, syndromes, stomatognathic systemdiagnóstico, niño, odontología, odontología pediátrica, odontólogos, patología oral, medicina oral, síndromes, síndrome Cri du Chat, síndrome del maullido del gato, semiología oral, sistema estomatognáticocriança, dentistas, diagnósticos, medicina oral, odontologia, odontopediatria, patologia oral, semiologia oral, síndrome, síndrome do choro do gato, síndrome de Cri-du-Chat, sistema estomatognático

References
1. Saldarriaga W, Collazoz-Saa L, Ramirez-Cheyne J. Cri-du-Chat syndrome diagnosed in a 21-year-old woman by means of comparative genomic hybridization. Rev Fac Med. 2017; 65(3): 525-529. http://doi.org/10.15446/revfacmed.v65n3.57414
2. Yáñez-Vico R, Rodríguez-Caballero Á, Iglesias-Linares A, Guerra-López N, Torres-Lagares D, Machuca-Portillo G. Craniofacial characteristics in cri-du-chat syndrome. Oral Med Oral Pathol Oral Radiol Endod. 2010; 110(6). http://doi.org/10.1016/j.tripleo.2010.08.021
3. Carbajo-Vélez M. Síndrome del maullido del gato. Intervención educativa. TABANQUE Rev Pedagog. 2012; 25: 235-250.
4. Rodríguez-Caballero A, Torres-Lagares D, Rodríguez-Pérez A, Serrera-Figallo MA, Hernández-Guisado JM, Machuca-Portillo G. Cri du chat syndrome: a critical review. Med Oral Patol Oral Cir Bucal. 2010 may; 15(3): 473-478. http://doi.org/10.4317/medoral.15.e473
5. Martín-Sanjuan C, Moreno-Martin C, de los Ríos JM, Urberuaga M, Domingo R. Consideraciones dentales en el síndrome de maullido de gato: a propósito de tres casos. Cient Dent. 2008 abr; 5(1): 45-48.
6. Corcuera-Flores JR, Casttellanos-Cosano L, Torres-Lagares D, Serrera-Figallo MÁ, Rodríguez-Caballero Á, Machuca-Portillo G. A systematic review of the oral and craniofacial manifestations of Cri du chat syndrome. Clin Anat. 2016; 29(5): 555-60. http://doi.org/10.1002/ca.22654
7. Martínez-Fernández M, Aceña M, McDonald A, Centeno-Malfaz F, Delicado A, Palomares M, Lapunzina P, Martínez Frías M. Paciente con síndrome de Cri-Du-Chat y de Beckwith-Wiedemann originados por un derivado de translocación paterna. Rev Dismorfol Epidemiol. 2009; 5(8).
8. Honjo R, Mello C, Pimenta E, Núñez E, Benedetto L, Khoury R, et al. Cri du Chat syndrome: Characteristics of 73 Brazilian patients. J Intellect Disab Res. 2018. http://doi.org/10.1111/jir.12476
9. Esparza-García E, Cárdenas-Conejo A, Huicochea-Montiel JC, Aráujo-Solís M. Cromosomas, cromosomopatías y su diagnóstico. Rev Mex Pediatr. 2017; 84(1): 30-39.
10. Cerruti-Maindari P. Cri du Chat syndrome. Orphanet J Rare Dis. 2006 Sep; 1(33): 1-9. https://doi.org/10.1186/1750-1172-1-33
11. Elmakky A, Carli D, Lugli L, et al. A three-generation family with terminal microdeletion involving 5p15.33-32 due to a whole-arm 5;15 chromosomal translocation with a steady phenotype of atypical cri du chat syndrome. Eur J Med Genet. 2014; 57(4): 145-150. https://doi.org/10.1016/j.ejmg.2014.02.005
12. Ochoa-Gómez L, Orden-Rueda C, Ruiz del Olmo JI, Clavero-Montañes N, Berdún-Cheliz E, Sánchez-Gimeno J. Síndrome Cri du Chat: a propósito de un caso. Características clínicas y evolutivas. Rev Español Pediatr. 2017; 73(2): 109-111.
13. Parra J, Peña M, Tamayo V, Fernández I, Peña L. Síndrome de maullido de gato o “Cri Du Chat”. Presentación de un caso. Rev Pediatr Electron. 2012; 9(1).
14. Santana Hernández E, Tamayo Chang V, Bruzón-Hernández M. Síndrome de 5p menos. Presentación de un caso. Medisur. 2014 oct; 12(4).
15. Kim KM, Kim JD. Effects of oral stimulation intervention in newborn babies with Cri du Chat syndrome: Single-Subject Research Design. Occupat Therapy Internat. 2018 May: 1-8. http://doi.or/10.1155/2018/6573508
16. Galo BL, Alvarenga R. Síndrome de Cri du Chat, una rara cromosopatía. Rev Med Hondur. 2012; 80(1).
17. Pereira J, Oliveira R, Lindemann D, de Araújo F, Almeida J. Cri-du-Chat syndrome: conservative dental treatment in an 8-year old child. Stomatos. 2013 jun; 19(36).
18. Rodríguez A, Torres D, Yáñez R, Gutiérrez J, Machuca G. Assessment of orofacial characteristics and oral pathology associated with cri-du-chat syndrome. Oral Dis. 2012; 18. https://doi.org/10.1111/j.1601-0825.2011.01864.x
19. Mainardi PC, Pastore G, Castronovo C, et al. The natural history of Cri du Chat Syndrome. A report from the Italian Register. Eur J Med Genet. 2006; 49(5): 363-383. https://doi.org/10.1016/j.ejmg.2005.12.004
20. Gómez E, Olivar A, García E, Domínguez M, Arias B. Manejo inicial del síndrome de Cri du Chat. Vox Pediatr. 2011; 18(1): 97-100.
21. Páez C, Borsatto M, Mussolino A, Campos F, Orsi I. Cri du Chat syndrome: A case report. Spec Care Dentist. 2005; 25(6).
22. Ballesta S, Machuca G, Torres D, Rodríguez A, Yañez R, Solano E, Perea E. Determination of periodontopathogens in patients with Cri du chat syndrome. Med Oral Patol Oral Cir Bucal. 2013 nov; 18(6): 883-887. https://doi.org/10.4317/medoral.19400
23. Liverani ME, Spano A, Danesino C, Malacarne M, Cavani S, Spunton M, Guala A. Children and adults affected by Cri du Chat syndrome. Care’s recommendation. Pediatr Report. 2019; 11: 7839.
24. Molina-García A, Castellanos-Cosano L, Machuca-Portillo G, Posada-de la Paz M. Impact of rare diseases in oral health. Med Oral Patol Oral Cir Bucal. 2016 sep; 21(5): 587-594.
25. Vega L, Díaz A, Arcas G, Satorre J, Satorre S, González E. Cardiopatías asociadas a síndromes genéticos diagnosticados en pacientes pediátricos. Acta Med Centro. 2017; 11(4).
How to Cite
Viteri Rentería, A. A., Armas Vega, A. del C., Carrera Robalino, Álex E., Paltas Miranda, A. P., & Paltas Miranda, M. E. (2020). Cri Du Chat Syndrome: Considerations in Dentistry. A Systematic Review. Universitas Odontologica, 39. https://doi.org/10.11144/Javeriana.uo39.scdc
Section
Clinical Practice

Most read articles by the same author(s)