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Peg laterals typically occur on both sides, [2] and have short roots. [2] Inheritance may be involved, [ 2 ] and the frequency of microdontia in the upper laterals is just under 1%. [ 1 ] The second most commonly involved tooth is the maxillary third molars, [ 3 ] and after this supernumerary teeth .
The tooth at the end of each region was less genetically stable and hence more prone to absence. In contrast, the tooth most mesial in each region seemed to be more genetically stable. [9] A subsequent theory hypothesised the teeth at the end of each region were possibly "vestigial bodies" that became obsolete during the evolutionary process.
Turner's hypoplasia or Turner's tooth is a presentation of enamel hypoplasia that normally affects only a single tooth. Its causes can be the same as other forms of enamel hypoplasia, but it is most commonly associated with trauma to a primary maxillary central incisor and the subsequent developmental disturbance of the underlying permanent ...
Radiographically, affected teeth have short and narrow roots, and obliterated pulps due to dentine hypertrophy before or shortly after tooth eruption. [2] The severity of these features is variable, with some teeth presenting with total obliteration of the pulp, while other teeth appear to have normal, healthy dentine. [2]
As a tooth is forming, a force can move the tooth from its original position, leaving the rest of the tooth to form at an abnormal angle. Cysts or tumors adjacent to a tooth bud are forces known to cause dilaceration, as are primary (baby) teeth pushed upward by trauma into the gingiva where it moves the tooth bud of the permanent tooth. [67]
However, the position on the crown, the tooth type and the cause of the disruption are all likely contributing factors. It has been suggested that because it is relatively rare to have both linear enamel hypoplasia and PEH, these types of defects may be commonly caused by different factors. [5]
It’s a comparatively small snake, with a short, stout body measuring 1–3 feet and weighing less than one pound. Their body colors are shades of brown, gray, reddish-orange, or olive, with ...
Dentin dysplasia (DD) is a rare genetic developmental disorder affecting dentine production of the teeth, commonly exhibiting an autosomal dominant inheritance that causes malformation of the root. It affects both primary and permanent dentitions in approximately 1 in every 100,000 patients. [ 1 ]