Results 81 to 90 of about 15,328 (193)

Compromised alveolar bone cells in a patient with dentinogenesis imperfecta caused by DSPP mutation

, 2018
International audienceDentin sialophosphoprotein (DSPP) plays an important role in the mineralization of both dentin and bones. The Dspp null mice developed periodontal diseases. Patients with DSPP mutations have dentinogenesis imperfecta (DGI), but very
Thantrira Porntaveetus, Theerapanon, Thanakorn, Osathanon, Thanaphum, Suphapeetiporn, Kanya, Porntaveetus, Thantrira, Nowwarote, Nunthawan, Kittisak Sanon, Nunthawan Nowwarote, Pavasant, Prasit, Shotelersuk, Vorasuk, Kanya Suphapeetiporn, Vorasuk Shotelersuk, Sanon, Kittisak, Srisawasdi, Sirivimol, Thanaphum Osathanon, Prasit Pavasant, Lawan Boonprakong, Sirivimol Srisawasdi, Thanakorn Theerapanon, Boonprakong, Lawan   +19 more
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Osteogenesis Imperfecta: An Overview [PDF]

, 2022
Osteogenesis Imperfecta (OI) or commonly referred to as brittle bone disease is a congenital connective tissue formation disorder characterized by bone fragility, osteopenia, skin disorders, blue sclera, dentinogenesis imperfecta (DI), and hearing loss ...
Rahma Ira Mustikasari, -, Nur Rochmah, -, Muhammad Faizi, -, Qurrota Ayuni Novia Putri, -   +3 more
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Dentinogenesis imperfecta: A review

, 2022
Dentinogenesis imperfecta (DGI) is an inherited dentin disease resulting in fragile teeth that affect the primary and permanent dentitions. It causes physical and aesthetic problems, including tooth discoloration and staining, and is responsible for ...
Carinci F.
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A Novel Mutation in the DSPP Gene Associated with Dentinogenesis Imperfecta Type II

, 2009
Hereditary dentin defects are divided into dentinogenesis imperfecta and dentin dysplasia. We identified a family segregating severe dentinogenesis imperfecta.
Jeon, D., Lee, H., Lee, S.-H., Lee, G., Jung, Y.-J., Lee, K.-E., Kim, J.-W., Shin, C.-U., Hahn, S.-H., Lee, S.-K.   +9 more
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Nanoscale arrangement of the healthy dentin and comparison with the dentino-genesis imperfecta-affected dentin

International audienceConclusions Dentinogenesis Imperfecta ...
Riou, Margot, Vallet, Maxime, Vennat, Elsa, Leclercq, Margot   +3 more
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Oral Health-Related Quality of Life in Dutch Adults With Osteogenesis Imperfecta [PDF]

Objective: To explore the oral health-related quality of life and its possible risk factors among adults with Osteogenesis Imperfecta using the Oral Health Impact Profile (OHIP)-49 questionnaire.
de Kuijper, Maurits, Appelman-Dijkstra, Natasha M., Appelman-Dijkstra, N.M., Zillikens, M.C., Janus, G.J.M., Kuijper-Timmermans, E. de, Blokland, L., de Kuijper-Timmermans, Emmanuelle, Kuijper, M. de, Gooijer, Koert, Janus, Guus J. M., Blokland, Lieke, Zillikens, M. Carola, Harsevoort, Arjan, Harsevoort, A., Gooijer, K., Kalaykova, Stanimira, Kalaykova, S., Janus, A.J.M., Appelman‐Dijkstra, Natasha M., Janus, Guus, Zillikens, Carola, Appelman-Dijkstra, Natasha, de Kuijper‐Timmermans, Emmanuelle   +23 more
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THE CONTRIBUTION OF KINETIC THERAPY IN LOBSTEIN’S DISEASE [PDF]

Annals of the “Ştefan cel Mare” University: Physical Education and Sport Section - The Science and Art of Movement, 2018
Osteogenesis imperfecta is a genetic disease of the connective tissue whose main clinical sign is increased bone fragility, manifested especially through fractures of the long limbs. OI presents major clinical signs and minor clinical signs.
Sergiu Danail, Danelciuc Francisc Tadeus
doaj  

Alternative treatment for dentinogenesis imperfecta

Revista Cubana de Estomatología, 2015
Introduction: Dentinogenesis imperfecta is an autosomal dominant hereditary disease originated in the stage of histodiferenciation during the odontogenesis, it´s a form of a localized mesodermic dysplasia, characterized by alteration of dentinal proteins.
Mirta Elena Montero del Castillo, Yanet Casals González, Lourdes Valdés Barroso   +2 more
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FAMILY SURVEILLANCE OF OSTEOGENESIS IMPERFECTA: PREGNANCY OUTCOMES, TACTICAL APPROACHES, AND PROSPECTS FOR SOLVING THE PROBLEM

Мать и дитя в Кузбассе, 2023
Osteogenesis imperfecta is a rare, hereditary, genetically heterogeneous disease of connective tissue and skeleton caused by mutation of genes encoding collagen, osteoblast differentiation, bone tissue remodulator proteins and many other genes.
Сергей Васильевич Матошин, Светлана Владимировна Шрамко   +1 more
doaj  

Dentinogenesis Imperfecta Type I and II: A Case Series Highlighting Clinical and Radiographic Insights

Indian Journal of Dental Sciences
Dentinogenesis imperfecta (DI) is a rare hereditary disorder affecting the dentin structure of both primary and permanent teeth, characterized by discoloration, structural fragility, and distinctive radiographic features.
K. Kavitha, Parikh J. Shilpa, Shah S. Jigna   +2 more
doaj   +1 more source