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Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes
Oligodontia is defined as the congenital lack of six or more permanent teeth, excluding third molars. Oligodontia as well as hypodontia (lack of one or more permanent teeth) are highly heritableExpand
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WNT10A mutations account for ¼ of population‐based isolated oligodontia and show phenotypic correlations
A large proportion (>50%) of patients with isolated oligodontia were recently reported with WNT10A mutations. We have analyzed a population‐based cohort of 102 individuals diagnosed withExpand
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Signs and symptoms from ectodermal organs in young Swedish individuals with oligodontia.
OBJECTIVES The aim was to assess signs and symptoms from other ectodermal organs in addition to teeth in young individuals with oligodontia and to establish the prevalence of oligodontia. SAMPLEExpand
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Using the International Classification of Functioning, Disability and Health (ICF) to Describe Children Referred to Special Care or Paediatric Dental Services
Children in dentistry are traditionally described in terms of medical diagnosis and prevalence of oral disease. This approach gives little information regarding a child’s capacity to maintain oralExpand
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Chronic recurrent multifocal osteomyelitis involving both jaws: report of a case including magnetic resonance correlation.
A case of chronic recurrent multifocal osteomyelitis in a 14-year-old girl is presented. The disease had an initial aggressive osteolytic appearance involving both the maxilla and the mandible.Expand
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Studies on the relationship between changes in radiographic bone height and probing attachment.
The aim of this investigation was to determine the relationship between loss of radiographic crestal bone height and probing attachment loss. As part of this aim, we are introducing a new method forExpand
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Further evidence for specific IFIH1 mutation as a cause of Singleton–Merten syndrome with phenotypic heterogeneity
Singleton–Merten syndrome (MIM 182250) is an autosomal dominant inherited disorder characterized by early onset periodontitis, root resorption, osteopenia, osteoporosis, and aortic valve or thoracicExpand
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Oral health, medical diagnoses, and functioning profiles in children with disabilities receiving paediatric specialist dental care – a study using the ICF-CY
Abstract Purpose: To describe 0–16-year-old children with disabilities receiving paediatric specialist dental care from a biopsychosocial perspective, with focus on relationship between oral health,Expand
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Isolated oligodontia associated with mutations in AXIN2, MSX1, PAX9, and EDARADD
The general aim of this thesis was to broaden our knowledge of the signs and symptoms, genetics, and outcomes of dental implant treatment in individuals with oligodontia or ectodermal dysplasia.Expand
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Clinical, microbiological, and histological factors which influence the success of regenerative periodontal therapy.
The primary objectives of this double-blind, controlled clinical trial were to assess factor(s) which affect the success of guided tissue regeneration (GTR) procedures in mandibular Class II buccalExpand
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