Tiol-Carrillo A

Language: Spanish
References: 16
Page: 283-289
PDF size: 177.29 Kb.

ABSTRACT

Introduction: Peutz-Jeghers Syndrome (PJS) is a genetic alteration with oral manifestations through brown or blackish spots that spread over the skin and oral mucosa during the first years of life; it is also a high risk of developing gastrointestinal polyps that can lead to intestinal obstruction and ischemic intestinal damage to the colon, which can lead to death. Objective: To describe the clinical manifestations of PJS through a review of the literature and the presentation of a clinical case. Results: The etiology as well as the most characteristic systemic and oral manifestations of PJS, are exposed and correlate with the clinical case of an 11-year-old male patient. Conclusions: Numerous genetic diseases with specific craniofacial and oral manifestations require the stomatologist to have the minimum knowledge necessary to identify them; such is the case of PJS, which presents peri and intraoral affections known as mucocutaneous melanosis, pathognomonic findings of this condition.

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