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Results 1 - 10 of 30 for Tooth agenesis
  1. Keratoderma with woolly hair 
    ... Registry: Cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis Genetic Testing Registry: Wooly hair-palmoplantar keratoderma syndrome ...
    https://medlineplus.gov/.../condition/keratoderma-with-woolly-hair - Genetics
  2. Oculodentodigital dysplasia 
    ... to 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 features of this condition include ...
    https://medlineplus.gov/.../condition/oculodentodigital-dysplasia - Genetics
  3. Laryngo-onycho-cutaneous syndrome 
    ... its other functions leads to the nail and tooth abnormalities that occur in this condition. LAMA3 This condition ...
    https://medlineplus.gov/.../laryngo-onycho-cutaneous-syndrome - Genetics
  4. Weyers acrofacial dysostosis 
    ... called Ellis-van Creveld syndrome. In addition to tooth and nail abnormalities, people with Ellis-van Creveld syndrome have very ...
    https://medlineplus.gov/.../condition/weyers-acrofacial-dysostosis - Genetics
  5. Ellis-van Creveld syndrome 
    ... Ellis-van Creveld syndrome, Weyers acrofacial dysostosis involves tooth and nail abnormalities, although affected individuals have less pronounced short stature ...
    https://medlineplus.gov/.../condition/ellis-van-creveld-syndrome - Genetics
  6. Cockayne syndrome 
    ... symptoms often include hearing loss, vision loss, severe tooth decay, bone abnormalities, hands and feet that are cold all the ...
    https://medlineplus.gov/genetics/condition/cockayne-syndrome - Genetics
  7. Focal dermal hypoplasia 
    ... that 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
  8. Kallmann syndrome 
    ... cleft palate), abnormal eye movements, hearing loss, and abnormalities of tooth development. Some affected individuals have a feature called ...
    https://medlineplus.gov/genetics/condition/kallmann-syndrome - Genetics
  9. Mucopolysaccharidosis type IV 
    ... this 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
  10. Joubert syndrome 
    ... the cerebellar vermis and the brainstem. The molar tooth sign got its name because the characteristic brain abnormalities resemble the cross-section of a molar tooth ...
    https://medlineplus.gov/genetics/condition/joubert-syndrome - Genetics
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