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  2. Enamel hypoplasia - Wikipedia

    en.wikipedia.org/wiki/Enamel_hypoplasia

    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 ...

  3. Plane-form enamel hypoplasia - Wikipedia

    en.wikipedia.org/wiki/Plane-form_enamel_hypoplasia

    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].

  4. Linear enamel hypoplasia - Wikipedia

    en.wikipedia.org/wiki/Linear_enamel_hypoplasia

    ] 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.

  5. Pitting enamel hypoplasia - Wikipedia

    en.wikipedia.org/wiki/Pitting_enamel_hypoplasia

    One of the most common types, pitting enamel hypoplasia (PEH), ranges from small circular pinpricks to larger irregular depressions. [2] Pits also vary in how they occur on a tooth surface, some forming rows and others more randomly scattered. [3] PEH can be associated with other types of hypoplasia, but it is often the only defect observed. [4]

  6. Amelogenesis imperfecta - Wikipedia

    en.wikipedia.org/wiki/Amelogenesis_imperfecta

    People with amelogenesis imperfecta may have teeth with abnormal color: yellow, brown or grey; this disorder can affect any number of teeth of both dentitions. Enamel hypoplasia manifests in a variety of ways depending on the type of AI an individual has (see below), with pitting and plane-form defects common. [4]

  7. SLC13A5 citrate transporter disorder - Wikipedia

    en.wikipedia.org/wiki/SLC13A5_citrate...

    SLC13A5 citrate transporter disorder, or SLC13A5 Epilepsy, is a rare genetic spectrum disorder that presents with neurological symptoms. Symptoms include severe seizures, ataxia, dystonia, teeth hypoplasia, poor communication skills, difficulty standing or walking, as well as developmental delay. [1]

  8. Cleidocranial dysostosis - Wikipedia

    en.wikipedia.org/wiki/Cleidocranial_dysostosis

    The permanent teeth include supernumerary teeth. Unless these supernumeraries are removed they will crowd the adult teeth in what already may be an underdeveloped jaw. If so, the supernumeraries will probably need to be removed to make space for the adult teeth. Up to 13 supernumerary teeth have been observed. Teeth may also be displaced.

  9. Meige's syndrome - Wikipedia

    en.wikipedia.org/wiki/Meige's_syndrome

    Meige's syndrome is a type of dystonia.It is also known as Brueghel's syndrome and oral facial dystonia.It is actually a combination of two forms of dystonia, blepharospasm and oromandibular dystonia (OMD).