Results 21 to 30 of about 2,152 (168)
An unusual variation of radicular dentin dysplasia: A rare case report with review of literature
Indian Journal of Dental Research, 2020 Dentin dysplasia (DD) is a rare autosomal dominant disorder of dentin development, which is generally divided into two types based on the clinical and radiographic appearance of the affected dentinal tissues: Type-I (Radicular DD) and Type-II (Coronal DD)
Arun K Patnana +2 more
doaj +1 more source
Dentin dysplasia type 1d: A rare case
Indian Journal of Dental Research, 2014 Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by a defective dentin development with clinically normal-appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts.
Sujit Ranjan Sahoo, Sonia Aggarwal
doaj +1 more source
Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia [PDF]
Orphanet Journal of Rare Diseases, 2008 Abstract The hereditary dentine disorders, dentinogenesis imperfecta (DGI) and dentine dysplasia (DD), comprise a group of autosomal dominant genetic conditions characterised by abnormal dentine structure affecting either the primary or both the primary and secondary dentitions. DGI is reported to have an incidence of 1 in 6,000 to 1 in 8,000,
Barron, Martin J. +3 more
openaire +4 more sources
Amyloid-mediated remineralization for tooth hypoplasia of cleidocranial dysplasia
Frontiers in Cellular and Infection Microbiology, 2023 IntroductionCleidocranial dysplasia (CCD) is an autosomal-dominant, heritable skeletal and dental disease, involving hypoplastic clavicles, defective ossification of the anterior fontanelle, dentin and enamel hypoplasia, and supernumerary teeth, which ...
Xiaohe Guo +8 more
doaj +1 more source
Dentin dysplasia type I: a case report and review of the literature
Journal of Medical Case Reports, 2010 Introduction Dentin dysplasia is a rare hereditary disturbance of dentin formation characterized by defective dentin development with clinically normal appearing crowns, severe hypermobility of teeth and spontaneous dental abscesses or cysts ...
Mirkarimi Mahkameh +3 more
doaj +1 more source
Dental Research Journal, 2014 Dentin dysplasia is an exceptionally rare, autosomal-dominant, hereditary condition, primarily characterized by defective dentin formation affecting both the deciduous and permanent dentitions.
Sowmya Nettem +3 more
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Dental Manifestations and Oral Management of X-Linked Hypophosphatemia
Endocrines, 2022 X-linked hypophosphatemia (XLH) is the most common genetic form of rickets and osteomalacia and is characterized by growth retardation, deformities of the lower limbs, and bone and muscular pain.
Rena Okawa, Kazuhiko Nakano
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Mouse Dspp frameshift model of human dentinogenesis imperfecta
Scientific Reports, 2021 Non-syndromic inherited defects of tooth dentin are caused by two classes of dominant negative/gain-of-function mutations in dentin sialophosphoprotein (DSPP): 5′ mutations affecting an N-terminal targeting sequence and 3′ mutations that shift ...
Tian Liang +11 more
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Dentin dysplasia type I: a challenge for treatment with dental implants
Head & Face Medicine, 2007 Background Dentin dysplasia type I is characterized by a defect of dentin development with clinical normal appearance of the permanent teeth but no or only rudimentary root formation.
Meyer Ulrich +5 more
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Epidemiological and Clinical Features of Regional Odontodysplasia in South Korean Pediatric Patients: A Multicenter Case Series Study. [PDF]
Int J Paediatr DentABSTRACT Background Regional odontodysplasia (RO) is a rare developmental dental anomaly with unknown prevalence. Current knowledge is largely limited to individual case reports. Aim This study aims to present epidemiological data, clinical features, and radiographic characteristics of pediatric and adolescent patients with RO in South Korea. Design In
Lee SD +5 more
europepmc +2 more sources