Results 11 to 20 of about 14,453 (188)

Morphological Study of Dental Structure in Dentinogenesis Imperfecta Type I with Scanning Electron Microscopy [PDF]

Healthcare (Switzerland), 2022
Background: Dentinogenesis imperfecta type I (DGI-I) is a hereditary alteration of dentin associated with osteogenesis imperfecta (OI). Aim: To describe and study the morphological characteristics of DGI-I with scanning electron microscopy (SEM ...
Joaquin de Nova, Vicente Vera Gonzalez, Andrea Martín-Vacas   +2 more
exaly   +5 more sources

Esthetic-based Dental Management of Dentinogenesis Imperfecta in a 2.5-year-old Child [PDF]

Journal of Kerman University of Medical Sciences, 2021
Background: Dentinogenesis imperfecta (DI) is an autosomal dominant (AD) hereditary dentin disorder, which occurs in the absence of any systemic disorder. The patients with DI presented rapid and severe attrition in primary teeth, which causes functional
Leyli Sadri, Soroush Sadri, Najmeh Akhlaghi, hamid sarlak   +3 more
doaj   +5 more sources

Dentinogenesis imperfecta [PDF]

Medizinische Genetik, 2007
Zusammenfassung Unter Dentinogenesis imperfecta versteht man eine kongenitale Dysplasie des Dentins, die isoliert oder im Zusammenhang mit einer hereditären Allgemeinerkrankung wie der Osteogenesis imperfecta auftreten kann. Sie wird meist autosomal dominant vererbt und manifestiert sich klinisch in einer opaleszierenden Goldbraun- oder ...
Schulte, J M, Van Waes, H
core   +8 more sources

Genetic Aspects of Dentinogenesis Imperfecta

Journal of Dentistry Indonesia, 2015
Dentinogenesis Imperfecta (DI) is a hereditary, simple autosomal dominant disorder showing abnormalities in the dentin of the developing teeth and occurring at a rate of about 1 in 8000 births.
Elza Ibrahim Auerkari, Hedijanti Joenoes
doaj   +3 more sources

Clinical manifestations and dental management of dentinogenesis imperfecta associated with osteogenesis imperfecta: Case report

Saudi Dental Journal, 2013
Dentinogenesis imperfecta (DI) associated with osteogenesis imperfecta (OI) is a genetic disorder that affects the connective tissues and results in dentine dysplasia.
Halima Abukabbos, Faisal Al-Sineedi
exaly   +3 more sources

Analysis of Genetic Factors in a Family With Short Stature. [PDF]

Mol Genet Genomic Med
We identified pathogenic variants of two different genes, COL1A2 and GH1, in a family with short stature through trio‐WES, thereby providing a clear genetic diagnosis for this family. ABSTRACT Background To elucidate the genetic underpinnings of short stature in a familial cohort of five individuals.
Zhang S, Zuo T, Deng Y, Zhao D, Liao L.
europepmc   +2 more sources

Unravelling the Genetic Basis of Dentinogenesis Imperfecta

International Dental Journal, 2023
Aim or Purpose: Dentinogenesis imperfecta (DI) is an autosomal dominant genetic disorder affecting dentine formation. This study aimed to perform mutational analysis in individuals with DI to unravel its molecular mechanisms.
Dr Maleeha Gilani, Associate Professor Robert Anthonappa   +1 more
doaj   +2 more sources

Blue Sclera to Brittle Bones: A Rare Case of Osteogenesis Imperfecta With Dentinogenesis Imperfecta and Nephrocalcinosis [PDF]

Journal of Investigative Medicine High Impact Case Reports
Osteogenesis imperfecta (OI) is a rare genetic disorder characterized by bone fragility. Its association with dentinogenesis imperfecta (DI) is well documented, but the concurrent presentation with nephrocalcinosis is uncommon and poorly understood.
Saad Hayat BDS, Ahmad Roshan Mayan BDS, Malik WZ Khan MBBS, Qazi Jawad Hayat BDS   +3 more
doaj   +2 more sources

Prevalence of Dentinogenesis Imperfecta in a French Population. [PDF]

J Int Soc Prev Community Dent, 2017
Dentinogenesis imperfecta is a genetic disorder of the dentin occurring during the tooth development. It leads to many structural changes that can be identified clinically (brownish colored teeth, cracked enamel) and radiologically (globular crown, cervical constriction, short roots, and obliterated pulp chamber and/or root canals).
Cassia A, Aoun G, El-Outa A, Pasquet G, Cavézian R.   +4 more
europepmc   +4 more sources

Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report

Frontiers in Dentistry, 2016
Dentinogenesis imperfecta (DI) is a hereditary dentin defect caused by an autosomal dominant mutation in dentin sialophosphoprotein gene. Defective dentin development results in discolored teeth that are prone to wear and fracture.
Najmeh Akhlaghi, Ali-Reza Eshghi, Mehrnaz Mohamadpour   +2 more
doaj   +1 more source