
Amelogenesis Imperfecta: A Case Report
Author(s) -
Debanjali Mukherjee Mds
Publication year - 2020
Publication title -
clinical dentistry
Language(s) - English
Resource type - Journals
eISSN - 0974-4916
pISSN - 0974-3979
DOI - 10.33882/clinicaldent.14.25895
Subject(s) - amelogenesis imperfecta , enamel paint , amelogenin , dentistry , osteogenesis imperfecta , amelogenesis , medicine , orthodontics , ameloblast , anatomy
Amelogenesis imperfecta is a structural-developmental defect involving enamel. It may be hypoplastic, hypomaturation, or hypocalcified. Genetic mutation of enamel coding proteins noted in this heterogeneous group of hereditary disorder affecting both primary and permanent dentitions. Clinically the affected teeth depict discolouration, prone to disintegration and sensitivity. Radiological evaluation revealed very thin or absent of the enamel layer. Here, I am presenting a case report of amelogenesis imperfecta affecting a 19 year old, otherwise healthy, female patient. Key Words: Amelogenesis imperfecta, enamel, hypoplastic, Genetic mutation.