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Results 1 - 10 of 34 for Abnormal number of teeth
  1. FGFR2 gene 
    ... features. Affected individuals can have vision, hearing, and dental ... and deletions of a small number of nucleotides are also known to cause the ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
  2. FGFR1 gene 
    ... the roof of the mouth (a cleft palate), abnormal tooth development, and abnormalities of the hands and feet. ... called osteoglophonic dysplasia. People with this condition show abnormal bone ... They may also lack teeth, or their teeth may not appear until later ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics
  3. 48,XXYY syndrome 
    ... nondisjunction results in a reproductive cell with an abnormal number of chromosomes. In 48,XXYY syndrome, the extra ...
    https://medlineplus.gov/genetics/condition/48xxyy-syndrome - Genetics
  4. LAMA3 gene 
    ... features of LOC syndrome include malformed nails and abnormal teeth.The mutations involved in LOC syndrome lead to ...
    https://medlineplus.gov/genetics/gene/lama3 - Genetics
  5. Osteoglophonic dysplasia 
    ... Chang L, Cai S, Lu YG, Xu L. Abnormal eruption of teeth in relation to FGFR1 heterozygote mutation: a rare case of osteoglophonic dysplasia with 4-year follow-up. BMC Oral Health. 2022 Feb 11;22(1):36. doi: 10.1186/s12903-022-02069-6. Citation on PubMed
    https://medlineplus.gov/genetics/condition/osteoglophonic-dysplasia - Genetics
  6. Pol III-related leukodystrophy 
    ... during movement and at rest.Development of the teeth (dentition) is often abnormal in Pol III-related leukodystrophy, resulting in the absence of some teeth (known as hypodontia or oligodontia). Some affected infants ...
    https://medlineplus.gov/.../condition/pol-iii-related-leukodystrophy - Genetics
  7. Gray platelet syndrome 
    ... granules, platelets are unusually large and fewer in number than usual (macrothrombocytopenia). The abnormal platelets also appear gray when viewed under a ...
    https://medlineplus.gov/genetics/condition/gray-platelet-syndrome - Genetics
  8. Cranioectodermal dysplasia 
    ... The most common features involve bone abnormalities and abnormal development of certain tissues known as ectodermal tissues, which include the skin, hair, nails, and teeth. The signs and symptoms of this condition vary ...
    https://medlineplus.gov/.../condition/cranioectodermal-dysplasia - Genetics
  9. FGFR3 gene 
    ... syndrome. The main features of LADD syndrome are abnormal tear production, malformed ears with hearing loss, decreased saliva production, small teeth, and hand deformities. The FGFR3 gene variant that ...
    https://medlineplus.gov/genetics/gene/fgfr3 - Genetics
  10. Trichorhinophalangeal syndrome type I 
    ... lip (philtrum); a thin upper lip; and small teeth that are either decreased (oligodontia) or increased (supernumerary) in number. Almost all affected individuals have sparse scalp hair. ...
    https://medlineplus.gov/.../trichorhinophalangeal-syndrome-type-i - Genetics
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