نتایج جستجو برای: amelogenesis imperfecta

تعداد نتایج: 5103  

Journal: :Critical Reviews in Oral Biology & Medicine 2003

Background and Objectives: Jalili syndrome is a rare autosomal recessive genetic disorder, which so far, only 33 families with this disorder have been reported worldwide. Patients with this disease simultaneously develop cone-rod retinal dystrophy (CRD) and amelogenesis imperfecta (AI). In this study, a mutation causing Jalili syndrome, was investigated in an Iranian family.   Case Report: The...

2011
Pinky Satyajith Naik Shashikiran ND

This clinical report describes the oral rehabilitation of a very young child diagnosed with hypoplastic amelogenesis imperfecta. The specific treatment objectives being adequate patient management, eliminate tooth sensitivity while enhancing esthetics, masticatory function and improved self confidence. The treatment included full mouth rehabilitation with stainless steel crowns on posterior tee...

Journal: :Journal of prosthodontics : official journal of the American College of Prosthodontists 1997
G A Thompson J M Schwartz

A patient with Type I hypoplastic patterned amelogenesis imperfecta, subtype D, presented for prosthodontic evaluation. This article describes the developmental and pathophysiological background of this disease. A clinical report describing the diagnosis, treatment planning, and dental rehabilitation of the patient is reviewed.

2009
M. Švábová

Enamel anomalies – amelogenesis imperfecta, 1: 14000, several types with different heredity. Most frequent type is AD with hypomineralisation. Enamel matrix is normaly created, but the mineralisation is insufficient. The enamel is soft,peels off. Teeth are yellowbrown. Open bite is common. Reduction of pulp chamber occurs relatively early, so the reconstruction with crowns could be provided bef...

2013
Hans U. Luder Christina Gerth-Kahlert Silke Ostertag-Benzinger Daniel F. Schorderet

Jalili syndrome denotes a recessively inherited combination of an eye disease (cone-rod dystrophy) and a dental disorder (amelogenesis imperfecta), which is caused by mutations in the CNNM4 gene. Whereas the ophthalmic consequences of these mutations have been studied comprehensively, the dental phenotype has obtained less attention. A defective transport of magnesium ions by the photoreceptors...

2017
Anca Jivanescu Antonio Miglionico Souman Barua Simona Ioana Hategan

The Amelogenesis Imperfecta is associated with malocclusion and usually requires an interdisciplinary treatment. Due to the patient's refusal of orthodontic treatment, prosthodontics-based treatments alternative was considered and planned. The patient was treated with zirconia-based fixed partial dentures, which resulted in improved occlusion, better oral health, and improved esthetic appearance.

Journal: :Brazilian dental science 2013
Chiung-Fen Chen Jan Cc Hu Eduardo Bresciani Mathilde C Peters Maria Regina Estrella

Amelogenesis imperfecta (AI) is a group of inherited disorders primary affecting the structural of enamel. Patients with AI experience poor esthetic, excessive tooth sensitivity and compromised chewing function that dental treatments are frequently required at early age. This review describes the non-enamel implications, stage-specific management strategies and outcomes of selected restorative ...

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