Disturbances of dental development distinguish patients with oligodontia-ectodermal dysplasia from isolated oligodontia
نویسندگان
چکیده
منابع مشابه
[Oligodontia in 2 siblings with ectodermal dysplasia].
Oligodontia, a form of hypodontia, is commonly seen in permanent than in deciduous dentition. It is defined as the congenital absence of six or more teeth, excluding third molars. It is relatively a rare condition which occurs as an isolated finding or as part of a syndrome. The present paper shows a rare case of oligodontia with ectodermal dysplasia in 2 siblings (boys). Both the cases were as...
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Prosthodontists can serve as productive members of the craniofacial team and can help coordinate multidisciplinary treatment of patients with congenital anomalies. Often there are few, if any, evidence-based criteria to assist them in developing “correct” clinical protocols. When syndromes involve hypodontia, oligodontia, or anodontia, coordinating prosthetic treatment through phases of three-d...
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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. Article I is a population-based study in three Swedish counties of 162 individuals with oligodontia, which was a prevalence of 0.09%. The intent was to explore ways for dentists to assess symptoms from ...
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This case report defines a case of isolated oligodontia of 9 and 10 permanent teeth in 9-year-old monozygotic twin sisters and gives information about the possible genetic and environmental etiology, related dental anomalies and treatment options. The twins have a negative family history of hypodontia and oligodontia in their parents, as well as their paternal and maternal grandmothers and firs...
متن کاملAcromelia‐oligodontia syndrome
This case report describes a patient with ankyloglossia, oligodontia, unilateral hypoplasia of the zygoma and mandible, along with bilateral distal reduction anomalies of his limbs without long bone abnormalities. This may represent a mild variant of oromandibular limb hypogenesis syndrome, expanding the phenotypic spectrum, or a previously unrecognized malformation syndrome.
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ژورنال
عنوان ژورنال: Orthodontics & Craniofacial Research
سال: 2017
ISSN: 1601-6335
DOI: 10.1111/ocr.12214