Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Osteogenesis Imperfecta Type III"'
Autor:
Heba Salah A. ElAbd, Mohamed Moghazy
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 17, Iss 2, Pp 197-200 (2016)
Background: Osteogenesis imperfecta is a genetic disorder of bones, which has different types. Type III is characterized by recurrent fractures, progressive bone deformities. Cardiac manifestation is one of the important extraskeletal manifestations.
Externí odkaz:
https://doaj.org/article/622fdc09a26a4d76a933424a1de23bed
Autor:
Aishwarya Nanjappa, Navin H Krishnamurthy, Nagarathna Chikkanarasaiah, Nimishabalakrishnan Vathariparambath
Publikováno v:
International Journal of Clinical Pediatric Dentistry
Aim and objective The aim and objective of this report is to describe the dental management of 11-year-old patient with type III osteogenesis imperfecta (OI). Background Osteogenesis imperfecta or brittle bone disease is caused by mutations in the co
Akademický článek
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Autor:
Benedikt Leidinger, Ioannis Delniotis
Publikováno v:
The American Journal of Case Reports
Patient: Male, 9 Final Diagnosis: Osteogenesis imperfecta type III Symptoms: Walking difficulties Medication: — Clinical Procedure: Osteotomies and realignment of bone deformity Specialty: Orthopedics and Traumatology Objective: Congenital defects/
NANOINDENTATION MEASUREMENT ON INTERSTITIAL AND OSTEON OF BONE WITH OSTEOGENESIS IMPERFECTA-TYPE III
Autor:
Khairul Salleh Basaruddin, N. A. Azizan, S. F. Khan, A. Shukrimi, A. R. Sulaiman, Mohd Hanafi Mat Som
Publikováno v:
Journal of Mechanical Engineering Research & Developments. 42:168-171
"Osteogenesis imperfecta (OI) is one of the genetic disorder which was characterized by bone fragility. Previous studies reported that there are several mechanical properties has been used to investigate the strength of OI bone. However, little data
Autor:
Mauro Celli, Filippo Maria Ranaldi, Lorena Martini, Anna Zambrano, Pietro Persiani, Ciro Villani, Patrizia D'Eufemia
Publikováno v:
Journal of Pediatric Orthopaedics B. 28:179-185
Osteogenesis imperfecta (OI) is a rare congenital osteodystrophy. Patients with OI present with osteoporosis, extreme bone fragility and severe deformities of the lower limbs, which predispose them to frequent fractures. The aim of our study is to de
Autor:
Efrat Fleissig, Adiel Barak
Publikováno v:
RETINAL Cases & Brief Reports. 13:43-46
Purpose To describe a case of scleral buckling in a patient with severe (Type III) osteogenesis imperfecta. Methods Single interventional case report of a 37-year-old woman, with clinically diagnosed osteogenesis imperfecta Type III, presenting with
Autor:
I. V. Komarova, E. G. Skryabin, M. A. Akselrov, S. N. Suprunets, A. N. Bukseev, D. A. Popkov, E. B. Khramova, I. I. Kukarskaya
Publikováno v:
Гений oртопедии, Vol 24, Iss 4, Pp 521-529 (2018)
The article presents a literature review on intrauterine bone fractures in fetuses suffering from osteogenesis imperfecta. Prenatal ultrasound investigation of the condition is made to identify pathologically changed bone tissue including shortened a
Autor:
Isabela Sica, Gustavo de Almeida Logar, Camila de Souza Arantes, Caio Peres Bellato, Milena Bezerra, C. Amaral
Publikováno v:
Arantes, C., Sica, I., Bezerra, M., Amaral, C., Bellato, C., & Logar, G. (2021). Osteogenesis imperfecta type III: Oral, craniofacial characteristics and atypical radiographic findings oral. Journal of clinical and experimental dentistry, 13(10), e1053–e1056.
Journal of Clinical and Experimental Dentistry
Journal of Clinical and Experimental Dentistry
Osteogenesis imperfecta (OI) is a disease characterized by decreased bone mineral density, causing susceptibility to bone fractures by mild trauma and bone deformities. The aim of this study was to describe an osteogenesis imperfecta type III clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::421db4ef2186e4335b9b1faba74c4681
https://hdl.handle.net/10550/87358
https://hdl.handle.net/10550/87358
Publikováno v:
Case Reports in Perinatal Medicine. 10
Objectives Thanks to the advances of modern medicine it has become possible to reach a fertile age even in the case of serious illnesses, enabling those patients to realize their desire to have children. This is also the case with the extremely heter