Results 101 to 110 of about 4,054 (202)
A Novel Splicing Mutation Alters DSPP Transcription and Leads to Dentinogenesis Imperfecta Type II [PDF]
, 2011 Dentinogenesis imperfecta (DGI) type II is an autosomal dominant disease characterized by a serious disorders in teeth. Mutations of dentin sialophosphoprotein (DSPP) gene were revealed to be the causation of DGI type II (DGI-II).
B Betz +26 more
core +3 more sources
Cukurova Medical Journal, 2017 Dentinogenesis imperfecta (DI) otozomal dominat genetik bir hastalıktır. Yüksek derecede penetrasyon ve düşük mutasyon oranına sahiptir. DI opalesant dentin ve dişlerde renk değişikliği ile karakterizedir. Dentin şiddetli yıpranmaya maruz kalabilir.
Shruthi RAO +5 more
doaj +1 more source
Study on frequency of dental developmental alterations in a MEXICAN school-based population [PDF]
, 2016 Background: The aim of this study was to know the distribution of dental developmental alterations in the population requesting stomatological attention at the Admission and Diagnosis Clinic of our institution in Mexico City.
Garcés Ortíz, Maricela +3 more
core +1 more source
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
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 +1 more
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 +2 more
doaj
Osteogenesis Imperfecta (Type IV) with Dental Findings in Siblings [PDF]
, 2011 Osteogenesis imperfecta (OI) is a hereditary disorder characterized by increased tendency for bone fractures due to high fragility. The clinical and radiological features of OI manifest in different age groups, although the disease is congenital in ...
Babu, Subhas +3 more
core +3 more sources
PROSTHODONTIC REHABILITATION OF A PATIENT WITH DENTINOGENESIS IMPERFECTA
annals and essences of dentistry, 2011 Dentinogenesis Imperfecta is an autosomal dominant disorder of tooth development characterized by the presence of opalescent dentin, resulting in a dusky blue to brownish discoloration of the teeth. This condition is genetically and clinically heterogeneous, it may affect only the teeth or it may be associated with the Osteogenesis Imperfecta.
Subbarayudu G +2 more
openaire +2 more sources
Familial dentinogenesis imperfecta, blue sclerae, and wormian bones without fractures: another type of osteogenesis imperfecta? [PDF]
, 1981 Peter Beighton
openalex +1 more source
Ultrastructure of Dentin Matrix in Heritable Dentin Defects [PDF]
, 1994 Heritable dentin defects form a group of diseases which exclusively affect dentin among the various dental tissues. While one type is associated with the generalized connective tissue disorder, osteogenesis imperfecta, other types occur as single traits.
Lukinmaa, P. -L., Ranta, H., Waltimo, J.
core +1 more source