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Results 1 - 10 of 14 for Enamel defects
  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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
  9. 48,XXYY syndrome 
    ... primary (baby) or secondary (adult) teeth, thin tooth enamel, crowded or misaligned teeth, and multiple cavities. Additionally, individuals with 48,XXYY syndrome may have flat feet (pes planus), elbow abnormalities, abnormal fusion of certain bones in the forearm ( ...
    https://medlineplus.gov/genetics/condition/48xxyy-syndrome - Genetics
  10. Oculofaciocardiodental syndrome 
    ... radiculomegaly) are characteristic of OFCD syndrome. Additional dental abnormalities can include delayed loss of primary (baby) teeth, missing or abnormally small teeth, misaligned teeth, and defective tooth enamel. OFCD syndrome is very rare; the incidence is ...
    https://medlineplus.gov/.../oculofaciocardiodental-syndrome - Genetics
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