Amelogenesis Imperfecta. Case Report

Overview

Journal Rev Cient Odontol (Lima)

Specialty Dentistry

Date 2024 Jan 30

PMID 38288452

Authors

Nicole Alessandra Herrera-Rojas

Guido Alberto Perona-Miguel de Priego

Affiliations

Soon will be listed here.

Abstract

The main origin of amelogenesis imperfecta (AI) is a genetic alteration inherited by a family member which affects the dental enamel of the teeth of a person with this condition in various ways. The present clinical case from the Teaching Dental Clinic of the Peruvian University Cayetano Heredia is of a 6-year 5-month-old male child who came to the dental office accompanied by his father and 8-year-old sister, diagnosed with the same AI condition. The comprehensive treatment proposed for this patient was determined by radiographic and clinical examinations and consultations with specialists in different areas. The purpose of this publication was to report a case and describe possible clinical approaches.

Citing Articles

Partial Amelogenesis Imperfecta: A Report of a Rare Case.

AlBagieh H, Alomran L, AlBishry F, Aloraini T, Almofarej N, Alhamzah N Cureus. 2024; 16(11):e73856.

PMID: 39583606 PMC: 11585384. DOI: 10.7759/cureus.73856.

Etiology, Classification, and Restorative Management of Amelogenesis Imperfecta Among Children and Young Adults: A Scoping Review.

Bin Saleh S Cureus. 2024; 15(12):e49968.

PMID: 38179349 PMC: 10765965. DOI: 10.7759/cureus.49968.

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