Results 31 to 40 of about 4,054 (202)

Dentinogenesis imperfecta: A review and case report of a family over four generations

Indian Journal of Dental Research, 2008
Dentinogenesis imperfecta (DGI) is one of the most common hereditary disorders of dentin formation. It follows an autosomal dominant pattern of transmission, affecting both the formation and mineralization of dentin.
Bhandari Sudhir, Pannu Karneev
doaj   +2 more sources

Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report. [PDF]

J Dent (Tehran), 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.
Akhlaghi N, Eshghi AR, Mohamadpour M.
europepmc   +1 more source

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   +3 more sources

Prosthetic Rehabilitation of Three Dentinogenesis Imperfecta Patients using Hobo Twin Stage Technique and Implant Supported Overdenture - A Case Report

Indian Journal of Dental Research
Rehabilitation of an attrited dentition is one of the most challenging task faced by a prosthodontist which requires a systematic, phase wise approach. Hobo’s techniques and Pankey Mann Schuyler’s philosophy are widely used and documented for full mouth ...
Amina, S Abirami, Geeta Rajput, Shaista Afroz, Shua Aftab   +4 more
doaj   +2 more sources

Oral manifestations and rehabilitation of a patient with osteogenesis imperfecta [PDF]

Srpski Arhiv za Celokupno Lekarstvo, 2021
Introduction. Osteogenesis imperfecta is a rare heritable connective tissue disorder characterized by increased fragility of the bony tissue. The incidence of orofacial alterations associated with osteogenesis imperfecta is variable and includes ...
Milanović Milena, Beloica Miloš, Jovičić Olivera, Mandinić Zoran, Janjić Bojan, Juloski Jelena   +5 more
doaj   +1 more source

Isolated dentinogenesis imperfecta: Novel DSPP variants and insights on genetic counselling. [PDF]

Clin Oral Investig
Hassib NF, Mehrez M, Mostafa MI, Abdel-Hamid MS.   +3 more
europepmc   +3 more sources

A homozygous SP7/OSX mutation causes osteogenesis and dentinogenesis imperfecta with craniofacial anomalies. [PDF]

JBMR Plus
Al-Mutairi DA, Jarragh AA, Alsabah BH, Wein MN, Mohammed W, Alkharafi L.   +5 more
europepmc   +3 more sources

The genetics of non-syndromic dentinogenesis imperfecta: a systematic review. [PDF]

Eur Arch Paediatr Dent
Gilani M, Saikia A, Anthonappa R.
europepmc   +2 more sources

A family study of dentinogenesis imperfecta shields type II caused by a novel DSPP mutation and investigations on the isolated stem cells from human exfoliated deciduous teeth. [PDF]

BMC Oral Health
Gao Q, Yue N, Liu K, Deng Z, Yang L, Zou J, Du Q.   +6 more
europepmc   +2 more sources

A Novel Mutation in the TRIP11 Gene: Diagnostic Approach from Relatively Common Skeletal Dysplasias to an Extremely Rare Odontochondrodysplasia

JCRPE, 2022
Odontochondrodysplasia (ODCD, OMIM #184260) is a rare, non-lethal skeletal dysplasia characterized by involvement of the spine and metaphyseal regions of the long bones, pulmonary hypoplasia, short stature, joint hypermobility, and dentinogenesis ...
Burcu Yeter, Ayca Dilruba Aslanger, Gözde Yeşil, Nursel H. Elçioğlu   +3 more
doaj   +1 more source