Results 61 to 70 of about 2,152 (168)

Personalized Bonding Approach for Full‐Mouth Adhesive Rehabilitation in Dentinogenesis Imperfecta

Clinical Case Reports, Volume 13, Issue 6, June 2025.
ABSTRACT Dentinogenesis imperfecta is a rare genetic disorder impacting dentin structure, with an incidence of 1 in 6000 to 1 in 8000 individuals. This condition alters the tooth's color and structure, affecting patients aesthetically, functionally, and socially.
Cyprien Clark, Olivia Kérourédan, Léa Massé   +2 more
wiley   +1 more source

Tissue Engineering and Regenerative Medicine: Perspectives and Challenges

MedComm, Volume 6, Issue 5, May 2025.
Tissue engineering and regenerative medicine. This review presents cell therapy, extracellular vesicle therapy, and tissue engineering in regenerative medicine, highlighting their key historical milestones, clinical applications, and current challenges.
Van T. Hoang, Quyen Thi Nguyen, Trang Thi Kieu Phan, Trang H. Pham, Nhung Thi Hong Dinh, Le Phuong Hoang Anh, Lan Thi Mai Dao, Van Dat Bui, Hong‐Nhung Dao, Duc Son Le, Anh Thi Lan Ngo, Quang‐Duong Le, Liem Nguyen Thanh   +12 more
wiley   +1 more source

Posttranslational Modification in Bone Homeostasis and Osteoporosis

MedComm, Volume 6, Issue 4, April 2025.
This review summarizes the updating researches concerning bone formation and bone resorption mediated by different types of posttranslational modification. We highlight dysregulated posttranslational modification in osteoblast and osteoclast differentiation. We then emphasize involvement of posttranslational modification in osteoporosis development, so
Yuzhe Lin, Shide Jiang, Yuming Yao, Hengzhen Li, Hongfu Jin, Guang Yang, Bingzhou Ji, Yusheng Li   +7 more
wiley   +1 more source

A rare condition affecting the primary and permanent dentition: Dentin dysplasia type I

Journal of Oral and Maxillofacial Radiology, 2013
Dentin dysplasia type I is a genetic defect of dentin formation, which is inherited as an autosomal dominant trait. In this anomaly, the teeth generally appear unremarkable with normal crowns; and it is characterized by normal appearing crowns, absence ...
Ahmet Ercan Sekerci, Meryem Etoz, Halil Sahman, Yildiray Sisman, Sinan Nazlim   +4 more
doaj  

Restorative treatment in a case of amelogenesis imperfecta and 9-year follow-up: a case report

Head & Face Medicine, 2020
Background Amelogenesis imperfecta is a hereditary malformation showing various manifestations regarding enamel dysplasia. This case report shows a 9-year follow-up after restorative treatment of a 16-year old female patient affected by a hypoplastic ...
Martin M. I. Sabandal, Till Dammaschke, Edgar Schäfer   +2 more
doaj   +1 more source

Incidence of Gingival Recessions in Adolescent Orthodontic Patients Treated With Fixed Appliances and Lingual Retainer

Journal of Clinical Periodontology, Volume 52, Issue 4, Page 589-598, April 2025.
ABSTRACT Aim To evaluate risk indicators for gingival recessions (GRs) in the lower anterior teeth of orthodontic patients post treatment and during a retention period of at least 5 years, compared to non‐treated controls. Material and Methods Eighty‐nine orthodontically treated patients who were recession‐free before treatment were recruited ...
Beatriz Celis, Javier Sanz‐Esporrin, Carina Verdasco, Rosa‐Maria Yañez‐Vico, Conchita Martin   +4 more
wiley   +1 more source

Dentinogenesis imperfecta type II in Swedish children and adolescents

Orphanet Journal of Rare Diseases, 2018
Background Dentinogenesis imperfecta (DGI) is a heritable disorder of dentin. Genetic analyses have found two subgroups in this disorder: DGI type I, a syndromic form associated with osteogenesis imperfecta (OI), and DGI type II, a non-syndromic form ...
K. Andersson, B. Malmgren, E. Åström, G. Dahllöf   +3 more
doaj   +1 more source

Case Report Of Dentinogenesis Imperfecta

International Dental Journal
Introduction: Dentinogenesis imperfecta is an autosomal-dominant genetic disorder characterized by marked aberrations in dentin mineralization and disorganized dentin architecture. This condition typically manifests across successive generations within a
Xu Laijun
doaj   +1 more source

Type I Dentin Dysplasia: The Literature Review and Case Report of a Family Affected by Misrecognition and Late Diagnosis. [PDF]

Medicina (Kaunas), 2023
Putrino A, Caputo M, Galeotti A, Marinelli E, Zaami S.   +4 more
europepmc   +1 more source

A novel DSPP mutation is associated with type II dentinogenesis Imperfecta in a chinese family

BMC Medical Genetics, 2007
Background Hereditary defects of tooth dentin are classified into two main groups: dentin dysplasia (DD) (types I and II) and dentinogenesis imperfecta (DGI) (types I, II, and III).
Xu Chengqi, Wang Xiaotao, Chang Wei, Zhao Zhen, Qu Erjun, Chen Lanying, Liu Jingyu, Zhang Xianqin, Wang Qing K, Liu Mugen   +9 more
doaj   +1 more source