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  2. Hypodontia - Wikipedia

    en.wikipedia.org/wiki/Hypodontia

    Hypodontia is defined as the developmental absence of one or more teeth excluding the third molars. It is one of the most common dental anomalies, and can have a negative impact on function, and also appearance. It rarely occurs in primary teeth (also known as deciduous, milk, first and baby teeth) and the most commonly affected are the adult ...

  3. Periodontal disease - Wikipedia

    en.wikipedia.org/wiki/Periodontal_disease

    Periodontal disease, also known as gum disease, is a set of inflammatory conditions affecting the tissues surrounding the teeth. [5] In its early stage, called gingivitis, the gums become swollen and red and may bleed. [5] It is considered the main cause of tooth loss for adults worldwide. [7][8] In its more serious form, called periodontitis ...

  4. Tooth loss - Wikipedia

    en.wikipedia.org/wiki/Tooth_loss

    Tooth loss. Tooth loss is a process in which one or more teeth come loose and fall out. Tooth loss is normal for deciduous teeth (baby teeth), when they are replaced by a person's adult teeth. Otherwise, losing teeth is undesirable and is the result of injury or disease, such as dental avulsion, tooth decay, and gum disease.

  5. Gum disease: causes, risks, prevention and when to see your ...

    www.aol.com/lifestyle/gum-disease-152133606.html

    The prevalence of gum disease is concerning as gingivitis and periodontitis can have serious consequences for your overall health. According to family dentist Kristy Gretzula, DMD, gum disease may ...

  6. Arts syndrome - Wikipedia

    en.wikipedia.org/wiki/Arts_syndrome

    Arts syndrome is a rare metabolic disorder that causes serious neurological problems in males due to a malfunction of the PRPP synthetase 1 enzyme. Arts Syndrome is part of a spectrum of PRPS-1 related disorders with reduced activity of the enzyme that includes Charcot–Marie–Tooth disease and X-linked non-syndromic sensorineural deafness.

  7. Dentinogenesis imperfecta - Wikipedia

    en.wikipedia.org/wiki/Dentinogenesis_imperfecta

    Dentinogenesis imperfecta. Dentinogenesis imperfecta (DI) is a genetic disorder of tooth development. It is inherited in an autosomal dominant pattern, as a result of mutations on chromosome 4q21, in the dentine sialophosphoprotein gene (DSPP). [1][2][3][4][5] It is one of the most frequently occurring autosomal dominant features in humans. [6]