Dentinogenesis Imperfekta : Aspek Genetika Molekular, Klasifikasi dan Upaya Penanggulangannya
Dentinogenesis Imperfecta (DI) is a hereditary simple autosomal dominant disorder showing abnormalities in the dentin of developing teeth and occuring at a rate of about 1 in 8000 births affecting both primary and secondary dentitions.
Elza Ibrahim Auerkari +2 more
doaj +1 more source
Elevated platelet counts in a cohort of children with moderate-severe osteogenesis imperfecta suggest that inflammation is present [PDF]
BACKGROUND: Elevated platelet counts are observed in cancer, autoimmunity and inflammation with concurrent illness. Proinflammatory cytokines are elevated in murine osteogenesis imperfecta (OI) models.
Bishop, N., Offiah, A.C., Salter, L.
core +1 more source
Knowledge and management of molar–incisor hypomineralisation amongst dentists in The Netherlands
Abstract Background Molar–incisor hypomineralisation (MIH) is a frequently encountered dental condition in the clinical setting, and correct diagnosis can influence management outcomes. Aim To assess the knowledge of and attitudes towards the management of MIH amongst dentists in the Netherlands.
Foteini Papanikolaou +5 more
wiley +1 more source
Brittle teeth with brittle bone in a family for four generations: Case report and literature review
Dentinogenesis imperfect (DI) is a hereditary dentine disorder affecting both deciduous and permanent teeth. DI is caused by mutations in genes encoding for type I collagen leading to discoloration of teeth.
P S Shilpa +4 more
doaj +1 more source
Disease‐Associated Factors at the Endoplasmic Reticulum–Golgi Interface
The ER–Golgi interface has garnered significant attention due to recent discoveries suggesting potential non‐vesicular transport mechanisms and regulation through liquid‐liquid phase separation. Numerous diseases linked to mutations in proteins located at this interface have been identified, highlighting the importance of comprehensive reviews in this ...
Miharu Maeda +2 more
wiley +1 more source
Timing of dental development in osteogenesis imperfecta patients with and without bisphosphonate treatment [PDF]
Peer ...
Arponen, Heidi +8 more
core +1 more source
Long‐Term Multidisciplinary Management of Regional Odontodysplasia: A Case Report
Regional odontodysplasia (RO) is a rare developmental anomaly involving both mesodermal and ectodermal dental tissues. It is characterized by hypoplasia and hypomineralization of enamel and dentin affecting a group of neighboring teeth and may involve primary, permanent dentition or both. Wide pulp chambers and thin, poorly defined hard tissue outlines,
Thalassia Niarchou +7 more
wiley +1 more source
Dentinogénesis imperfecta tipo II: Reporte de un caso
La Dentinogénesis Imperfecta es un desorden genético de carácter hereditario autosómico dominante, que se caracteriza por defectos en la dentina de ambas denticiones.
Magdalena-San Martín +3 more
doaj
Performing endodontic treatment on calcified root canals is highly challenging and time‐intensive. Even with the assistance of a dental operating microscope, the probability of iatrogenic errors is high. The aim of this report is to present successful endodontic treatments for severely calcified maxillary anterior teeth using a 3D endodontic sleeveless
Azadeh Hesarkhani +3 more
wiley +1 more source
Swellings over the Limbs as the Earliest Feature in a Patient with Osteogenesis Imperfecta Type V
Swellings over the upper and lower limbs were encountered in a one-year-old child. Skeletal survey showed a constellation of distinctive radiographic abnormalities of osteoporosis, hyperplastic callus and ossification of the interosseous membrane of the ...
Ali Al Kaissi +3 more
doaj +1 more source

