Dentinogenesis imperfecta [PDF]
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 +9 more sources
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
doaj +3 more sources
Blue Sclera to Brittle Bones: A Rare Case of Osteogenesis Imperfecta With Dentinogenesis Imperfecta and Nephrocalcinosis [PDF]
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 +3 more
doaj +2 more sources
Accidental Diagnosis of Type VII Osteogenesis Imperfecta in an Infant Presenting With Pneumonia and Rickets‐Like Rib Fractures: A Case Report [PDF]
ABSTRACT This case report describes a newborn diagnosed with Type VII Osteogenesis Imperfecta (OI) following an incidental finding of rib fractures during evaluation for pneumonia. The patient presented with multiple fractures, including deformities and callus formations in the ribs and extremities, initially raising concerns for differential diagnoses
Parviz S, Hooshyar D.
europepmc +2 more sources
Phenotypic Properties of Collagen in Dentinogenesis Imperfecta Associated with Osteogenesis Imperfecta [PDF]
Salwa Ibrahim,1,* Adam P Strange,2,* Sebastian Aguayo,2,3 Albatool Shinawi,1 Nabilah Harith,1 Nurjehan Mohamed-Ibrahim,1 Samera Siddiqui,2 Susan Parekh,1 Laurent Bozec4 1Department of Paediatric Dentistry, UCL Eastman Dental Institute, University College
Ibrahim S +8 more
doaj +2 more sources
Esthetic-based Dental Management of Dentinogenesis Imperfecta in a 2.5-year-old Child [PDF]
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 +3 more
doaj +3 more sources
Dental Management of a Child with Dentinogenesis Imperfecta: A Case Report [PDF]
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 +2 more
doaj +1 more source
Oral manifestations and rehabilitation of a patient with osteogenesis imperfecta [PDF]
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 +5 more
doaj +1 more source
Tratamiento integral y control a 12 años de paciente con Dentinogénesis Imperfecta tipo I
La Dentinogénesis Imperfecta es una anomalía dentaria determinada genéticamente y caracterizada clínicamente por una apariencia ámbar opalescente de la dentina.
Ingrid Clarisa Guitelman +2 more
doaj +1 more source
Minimally invasive orthodontics: elastodontic therapy in a growing patient affected by Dentinogenesis Imperfecta. [PDF]
AIM: The aim of the study was to report the use of an elastodontic therapy in a growing patient affected by Dentinogenesis Imperfecta, second class malocclusion, deep bite and lower arch crowding from the deciduous dentition to permanent one. CASE
Ierardo G +4 more
europepmc +3 more sources

