Results 81 to 90 of about 4,451 (219)

ISOLATED DENTINOGENESIS IMPERFECTA AND IN ASSOCIATION WITH OSTEOGENESIS IMPERFECTA – A LITERATURE REVIEW [PDF]

Romanian Medical Journal, 2018
Dental development is part of the craniofacial organogenesis, starting from the pluripotent cephalic neural crest cells, continuing with their movement towards the first pharyngeal arch and leading to the development of many elements of the ...
Andrei Kozma, Doriana Agop Forna, Viorica Radoi, Ana Maria Alexandra Stanescu, Radu Ursu, Laurentiu Camil Bohaltea   +5 more
doaj   +1 more source

Physiotherapy Intervention for Joint Hypermobility in Three Cases with Heritable Connective Tissue Disorders [PDF]

, 2010
peer reviewedIntroduction: In Joint Hypermobility Syndromes, chronic pain is the most disabling symptom. Its origin can be multiple (i.e. subluxations, sprains, pathologies of tendons, ligaments, peripheral nerves, multiple operations).
Crielaard, Jean-Michel, Croisier, Jean-Louis, Foidart-Dessalle, Marguerite, Forthomme, Bénédicte, Kaux, Jean-François, Toussaint, Geoffrey   +5 more
core   +1 more source

Effect of autoclave sterilization on nickel ion release from stainless steel crowns and space maintainer bands

European Journal of Oral Sciences, Volume 133, Issue 3, June 2025.
Abstract This study aimed to investigate the effect of autoclave sterilization on the leaching of nickel ions from stainless steel crowns and space maintainer bands used in pediatric dentistry. Sixty space maintainer bands and 60 stainless steel crowns were divided into sterilized (Amsco Century V‐120 Prevac steam sterilizer) and non‐sterilized groups.
Noura Alessa, Habah Alhamdan, Shahad Alrobaish, Nisrin AlQahtani, Norah Alarifi, Manal Almutairi, Latifa Alhowaish, Majedah Al‐Homaidhi, Reuof Alessa   +8 more
wiley   +1 more source

Dental Hard Tissue Study In A Hereditary Dentinogenesis Imperfecta Family

International Dental Journal
Aim or purpose: Hereditary dentinogenesis imperfecta is a rare autosomal dominant genetic disorder characterized by abnormal dentin structure, leading to impaired dental function and aesthetics.
Zhongren Deng, Yue Ning, Qin Du
doaj   +1 more source

A novel mutation in COL1A2 leads to osteogenesis imperfecta/Ehlers-Danlos overlap syndrome with brachydactyly

Genes and Diseases, 2019
Osteogenesis imperfecta (OI) is mainly characterized by bone fragility and Ehlers-Danlos syndrome (EDS) by connective tissue defects. Mutations in COL1A1 or COL1A2 can lead to both syndromes.
Thunyaporn Budsamongkol, Narin Intarak, Thanakorn Theerapanon, Somchai Yodsanga, Thantrira Porntaveetus, Vorasuk Shotelersuk   +5 more
doaj   +1 more source

Structural Variants in COL1A1 and COL1A2 in Osteogenesis Imperfecta

American Journal of Medical Genetics Part A, Volume 197, Issue 3, March 2025.
ABSTRACT Osteogenesis Imperfecta (OI) is a heterogeneous skeletal dysplasia characterized by bone fragility, skeletal deformities, and short stature. Most commonly, it is caused by autosomal dominant variants in the type I collagen genes, COL1A1 or COL1A2.
Dominyka Batkovskyte, Diana Swolin‐Eide, Anna Hammarsjö, Kristine Bilgrav Sæther, Sofia Thunström, Johanna Lundin, Jesper Eisfeldt, Anna Lindstrand, Ann Nordgren, Eva Åström, Giedre Grigelioniene   +10 more
wiley   +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

Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta

BMC Medical Genetics, 2011
Background Mutations in the FKBP10 gene were first described in patients with Osteogenesis imperfecta type III. Two follow up reports found FKBP10 mutations to be associated with Bruck syndrome type 1, a rare disorder characterized by congenital ...
Steinlein Ortrud K, Aichinger Eric, Trucks Holger, Sander Thomas   +3 more
doaj   +1 more source

Laporan Kasus: Dentinogenesis Imperfekta [PDF]

, 2019
Dentinogenesis imperfecta is the one of most common hereditary disorder of dentin formation, especially at histodifferentiation stage. It reported have to an incidences of 1 in 8000.
Abdurokhman, Evellyn Islami, Ashar, Fadli   +1 more
core   +2 more sources

Development, Disease, and Regeneration of Tissues in the Dental-Craniofacial Complex [PDF]

, 2013
This article has no ...
Chun, Yong-Hee P., Foster, Brian L, Lin, Zhao, Novince, Chad M., Paranjpe, Avina, Scheller, Erica L.   +5 more
core   +2 more sources