Results 81 to 90 of about 2,474 (180)

Dental Findings and Treatment in Osteogenesis Imperfecta: A Case Report

Selcuk Dental Journal
Osteogenesis imperfecta (OI) is a genetically inherited disease in which increased bone fragility, low bone mass, and connective tissue disorders are seen. In other words, 'glass bone disease'; has been associated with blue sclera, hearing problems, hand-
Yasemin İspir, Özge Anıl
doaj   +1 more source

Morphological and Ultrastructural Collagen Defects: Impact and Implications in Dentinogenesis Imperfecta. [PDF]

Dent J (Basel), 2023
Gadi LSA, Chau DYS, Parekh S.
europepmc   +1 more source

Clear Aligners in Patients with Amelogenesis and Dentinogenesis Imperfecta. [PDF]

Int J Dent, 2021
Sawan NM.
europepmc   +1 more source

Esthetic reconstruction of teeth in dentinogenesis imperfecta – A case report

, 2022
Gaurav Gupta, Dheeraj Gupta, Priyanka Gupta, Richa Gupta, Devanshi Sankhla   +4 more
openalex   +2 more sources

Osteogenesis imperfecta, a case report

Universidad Médica Pinareña, 2020
Introduction: osteogenesis imperfecta or crystal bones constitute the hereditary osteoporotic syndrome with the highest incidence in childhood. Case report: a 6-year and three-month-old school student admitted to the pediatric intensive care unit with a
Lázaro Raidel Moreira-Díaz, Yannyk Palenenzuela-Ramos, Jorge Enrique Padrón-Álvarez   +2 more
doaj  

Mouse Dspp frameshift model of human dentinogenesis imperfecta. [PDF]

Sci Rep, 2021
Liang T, Hu Y, Zhang H, Xu Q, Smith CE, Zhang C, Kim JW, Wang SK, Saunders TL, Lu Y, Hu JC, Simmer JP.   +11 more
europepmc   +1 more source

Dentinogenesis imperfecta: A review and case report of a family over four generations

Indian Journal of Dental Research, 2008
Dentinogenesis imperfecta (DGI) is one of the most common hereditary disorders of dentin formation. It follows an autosomal dominant pattern of transmission, affecting both the formation and mineralization of dentin.
Bhandari Sudhir, Pannu Karneev
doaj  

Non-Syndromic Dentinogenesis Imperfecta Caused by Mild Mutations in COL1A2. [PDF]

J Pers Med, 2021
Lee Y, Kim YJ, Hyun HK, Lee JC, Lee ZH, Kim JW.   +5 more
europepmc   +1 more source

Dentinogenesis imperfecta: The Genetic Causes and Outcomes

, 2021
Sydney Johnson
openalex   +2 more sources

A Novel Splicing Mutation Alters DSPP Transcription and Leads to Dentinogenesis Imperfecta Type II

, 2011
Jun Zhang, Jiucun Wang, Yanyun Ma, Wenqi Du, Siyang Zhao, Zuowei Zhang, Xiaojiao Zhang, Yue Liu, Huasheng Xiao, Hongyan Wang, Jin Li, Jie Liu   +11 more
openalex   +2 more sources