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Results 1 - 10 of 17 for Enamel defects
  1. ENAM gene 
    ... responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects. J Med Genet. 2003 Dec;40(12):900- ...
    https://medlineplus.gov/genetics/gene/enam - Genetics
  2. Amelogenesis imperfecta 
    ... responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects. J Med Genet. 2003 Dec;40(12):900- ...
    https://medlineplus.gov/genetics/condition/amelogenesis-imperfecta - Genetics
  3. Focal dermal hypoplasia 
    ... forms the protective outer layer of each tooth (enamel). Less commonly, abnormalities of the kidneys and gastrointestinal system are present. ...
    https://medlineplus.gov/genetics/condition/focal-dermal-hypoplasia - Genetics
  4. AMELX gene 
    ... other X chromosome to produce amelogenin. Their tooth enamel may have structural defects such as a distinctive pattern of vertical grooves. ...
    https://medlineplus.gov/genetics/gene/amelx - Genetics
  5. Mucopolysaccharidosis type IV 
    ... condition include mildly "coarse" facial features, thin tooth enamel, multiple cavities, heart valve abnormalities, a mildly enlarged liver (hepatomegaly), and a soft ...
    https://medlineplus.gov/.../condition/mucopolysaccharidosis-type-iv - Genetics
  6. Celiac disease 
    ... mineral density (osteoporosis), itchy skin rashes (dermatitis herpetiformis), defects in the enamel of the teeth, chronic fatigue, joint pain, poor ...
    https://medlineplus.gov/genetics/condition/celiac-disease - Genetics
  7. Vitamin D-dependent rickets 
    ... people with vitamin D-dependent rickets have dental abnormalities such as thin tooth enamel and frequent cavities. Poor muscle tone (hypotonia) and ...
    https://medlineplus.gov/.../condition/vitamin-d-dependent-rickets - Genetics
  8. Apert syndrome 
    ... dental problems, such as missing teeth, irregular tooth enamel, and crowded teeth.Many individuals with Apert syndrome have vision problems due to eye abnormalities, which can include bulging eyes (exophthalmos), wide-set ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  9. Oculodentodigital dysplasia 
    ... vision loss. Affected individuals also frequently have tooth abnormalities, such as small or missing teeth, weak enamel, multiple cavities, and early tooth loss. Other common ...
    https://medlineplus.gov/.../condition/oculodentodigital-dysplasia - Genetics
  10. Short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay 
    ... normal (hypodontia), and a lack of protective covering (enamel) on the surface of the teeth.Other signs and symptoms that have been reported in people with SHORT syndrome include immune system abnormalities, a kidney disorder known as nephrocalcinosis, hearing loss, ...
    https://medlineplus.gov/...ression-rieger-anomaly-and-teething-delay - Genetics
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