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Teeth displaying enamel hypoplasia lines, linear defects of enamel that form during crowns development as a result of periods of nutritional stress or disease during infancy and childhood Enamel hypoplasia is a risk factor for dental caries in children including early childhood caries (ECC), which continues to be a burden for many children.
Plane-form enamel hypoplasia is a dental condition that is distinguished by defects in the teeth enamel, that can occur due to genetic or environmental factors. It is common for the disease to occur during the developmental stages of the teeth, and childhood illnesses, such as respiratory infections, are often linked to disturbance of the enamel formation [5] [6].
] It is the most common type of enamel hypoplasia reported in clinical and archaeological samples, with other types including plane-form enamel hypoplasia and pitting enamel hypoplasia. [12] Linear enamel hypoplasia can be caused by a variety of factors, from genetic conditions to malnutrition and illnesses during childhood.
Pitting enamel hypoplasia, in an individual with amelogenesis imperfecta. It is not always clear why PEH forms instead of other hypoplasia types, particularly linear enamel hypoplasia. However, the position on the crown, the tooth type and the cause of the disruption are all likely contributing factors.
A delay in tooth development may also serve as an indication, whereby the absence of an adult successor slows down the normal resorption of the roots of the baby teeth, which is the progressive loss of parts of the tooth. Misplaced (ectopic) positioning of the adult teeth may be discovered upon examination or a radiograph.
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Enamel hypoplasia is a developmental defect of enamel that occurs during tooth development, mainly pre-natal or during early childhood. Teeth affected by enamel hypoplasia are at a higher risk of caries since there is an increased loss of minerals and therefore the tooth surface is able to breakdown more easily in comparison to a non ...
Molar incisor hypomineralisation (MIH) is a type of enamel defect affecting, as the name suggests, the first molars and incisors in the permanent dentition. [1] MIH is considered a worldwide problem with a global prevalence of 12.9% and is usually identified in children under 10 years old. [2]