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Results 1 - 8 of 8 for Abnormality of the dentition
  1. Oculofaciocardiodental syndrome 
    ... radiculomegaly) are characteristic of OFCD syndrome. Additional dental abnormalities can include the delayed loss of primary (baby) teeth, missing or abnormally small teeth, delayed teething (dentition), misaligned teeth, and defective tooth enamel.Individuals with ...
    https://medlineplus.gov/.../oculofaciocardiodental-syndrome - Genetics
  2. Pol III-related leukodystrophy 
    ... movement and at rest.Development of the teeth (dentition) is often abnormal in Pol III-related leukodystrophy, ... Affected individuals may be diagnosed with ataxia, delayed dentition, and hypomyelination (ADDH); hypomyelination, hypodontia, hypogonadotropic hypogonadism (4H ...
    https://medlineplus.gov/.../condition/pol-iii-related-leukodystrophy - Genetics
  3. POLR3A gene 
    ... coordination and balance (ataxia). Development of the teeth (dentition) is also abnormal in people with this disorder. ... Affected individuals may be diagnosed with ataxia, delayed dentition, and hypomyelination (ADDH); hypomyelination, hypodontia, and hypogonadotropic hypogonadism ( ...
    https://medlineplus.gov/genetics/gene/polr3a - Genetics
  4. POLR3B gene 
    ... with coordinating movements (ataxia). Development of the teeth (dentition) is also abnormal in this disorder.In the ... Affected individuals may be diagnosed with ataxia, delayed dentition, and hypomyelination (ADDH); hypomyelination, hypodontia, hypogonadotropic hypogonadism (4H ...
    https://medlineplus.gov/genetics/gene/polr3b - Genetics
  5. Craniometaphyseal dysplasia 
    ... bone formation in the jaw can delay teething (dentition) or result in absent (non-erupting) teeth. Infants ... mineralization, which may also contribute to the bone abnormalities.A mutation in the GJA1 gene causes some ...
    https://medlineplus.gov/.../condition/craniometaphyseal-dysplasia - Genetics
  6. MSX1 gene 
    ... and PAX9 reflect their role in patterning human dentition. Eur J Oral Sci. 2003 Oct;111(5): ...
    https://medlineplus.gov/genetics/gene/msx1 - Genetics
  7. Steatocystoma multiplex 
    ... NP. Steatocystoma multiplex, oligodontia and partial persistent primary dentition associated with a novel keratin 17 mutation. Br ...
    https://medlineplus.gov/genetics/condition/steatocystoma-multiplex - Genetics
  8. Camurati-Engelmann disease 
    ... in muscle mass and body fat, delayed teething (dentition), frequent cavities, delayed puberty, a shortage of red ...
    https://medlineplus.gov/.../condition/camurati-engelmann-disease - Genetics