Results 71 to 80 of about 2,152 (168)
Dentin dysplasia type I with pyogenic granuloma in a 12-year-old girl
This paper presents a case of dentin dysplasia, a rarely reported disorder that is also associated with pyogenic granuloma in a 12-year-old girl. The case presented as excessively mobile teeth that appeared radiographically as rootless teeth and also as ...
Nirmala SVSG, Sivakumar N, Usha K
doaj
Sequentially Functional And Asthetic Restoration Of Severe Dentin Dysplasia
Introduction: This case report introduced sequentially functional and aesthetic restoration on a patient with dentin dysplasia type II (DD-II) accompanied by severe tooth wear. Case description: An eight-year-old girl with severe tooth wear presented for
Xuemei Liu, Xu Chen
doaj +1 more source
Orthodontic movement of teeth with short root anomaly: should it be avoided, faced or ignored?
INTRODUCTION: Short Root Anomaly (SRA) is an uncommon disease and a challenge for orthodontic treatment as it tends to increase the risk of root resorption.
Jose Valladares Neto +2 more
doaj +1 more source
A dentin dysplasia differenciáldiagnosztikai nehézségei
Bizonytalan eredetű periapikális elváltozások megjelenésénél gondolnunk kell a dentin dysplasia lehetőségére. Differenciáldiagnosztikai szempontból lényeges felismerni ezt az örökletes kórképet, mert ez jelentősen befolyásolja a pácienstovábbi kezelését.
Komlós, György +4 more
openaire +2 more sources
Radiation Induced Hypoplasia of the Mandible and Retarded Tooth Development
Few cases of radiation-induced damage to the teeth and jaws, have been reported in the literature. Radiation therapy plays an important role in the treatment of patients affected with head and neck cancer.
Monica Tuteja +5 more
doaj
DSPP Gene Dsp Mutation Affects Dental Development
Aim or purpose: Hereditary dentin dysplasia is a common autosomal recessive genetic disease in oral health, and the DSPP gene is one of the main pathogenic genes.
Cai Haishen
doaj +1 more source
VPS4B mutation impairs the osteogenic differentiation of dental follicle cells derived from a patient with dentin dysplasia type I. [PDF]
Li Q +10 more
europepmc +1 more source
Novel frameshift mutations in DSPP cause dentin dysplasia type II. [PDF]
Lee JW +16 more
europepmc +1 more source
Dentin dysplasia type I-A dental disease with genetic heterogeneity. [PDF]
Chen D +5 more
europepmc +1 more source

