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Órgano Oficial de la Asociación Dental Mexicana

2021, Number 6

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Rev ADM 2021; 78 (6)

Gardner syndrome: case report and literature review.

Tiol-Carrillo A, Tiol-Morales A, Bahena-Martínez E

Language: Spanish
References: 10
Page: 356-360
PDF size: 306.97 Kb.


ABSTRACT

Gardner syndrome is a genetic disease of autosomal dominant inheritance, it presents multiple craniofacial manifestations characterized by bone overgrowths known as osteomas, risk of development of gastrointestinal polyps with high potencial of malignancy, and skin tumors or cysts, as well as dental alterations, among the characteristics of the presence of supernumerary teeth, dental retention, permanence of deciduous teeth and odontomas, the latter of great importance for the dentist. It is a disease that affects women and men indistinctly, however, its prevalence is higher in the female sex. The aim of this article is to explain the dental and craniofacial clinical and radiographic manifestations of Gardner syndrome by presenting a clinical case and a review of the literature.


REFERENCES

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  2. Pereira DL, Carvalho PA, Achatz MI, Rocha A, TardinTorrezan G, Alves FA. Oral and maxillofacial considerations in Gardner's syndrome: a report of two cases. Ecancermedicalscience. 2016; 10: 623.

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