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Results 1 - 10 of 13 for Craniosynostosis dental anomalies
  1. Hereditary hypophosphatemic rickets 
    ... can include premature fusion of the skull bones (craniosynostosis) and dental abnormalities. The disorder may also cause abnormal bone growth ...
    https://medlineplus.gov/.../hereditary-hypophosphatemic-rickets - Genetics
  2. MN1 C-terminal truncation syndrome 
    ... such as cone-shaped (conical ), jagged, or crowded teeth. Rarely, people with MCTT syndrome have premature fusion of certain skull bones (craniosynostosis). People with MCTT syndrome often have characteristic brain abnormalities. The surface of the brain normally has many ...
    https://medlineplus.gov/.../mn1-c-terminal-truncation-syndrome - Genetics
  3. Au-Kline syndrome 
    ... down the middle of the tongue. Less common abnormalities include premature ... teeth (oligodontia).Malformations of the heart, blood vessels, kidneys, ...
    https://medlineplus.gov/genetics/condition/au-kline-syndrome - Genetics
  4. Cranioectodermal dysplasia 
    ... tissues, which include the skin, hair, nails, and teeth. The signs and symptoms of ... craniosynostosis). A variety of facial abnormalities can occur in ...
    https://medlineplus.gov/.../condition/cranioectodermal-dysplasia - Genetics
  5. Carpenter syndrome 
    ... by the premature fusion of certain skull bones (craniosynostosis), abnormalities of the fingers and toes, and other developmental ... abnormal eye shape. Some affected individuals also have dental abnormalities including small primary (baby) teeth. Vision problems also ...
    https://medlineplus.gov/genetics/condition/carpenter-syndrome - Genetics
  6. Gorlin-Chaudhry-Moss syndrome 
    ... condition. Craniofacial dysostosis, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies, patent ductus arteriosus, and normal intelligence Craniofacial dysostosis, ...
    https://medlineplus.gov/.../condition/gorlin-chaudhry-moss-syndrome - Genetics
  7. FGFR2 gene 
    ... and symptoms of Antley-Bixler syndrome typically include craniosynostosis, distinctive facial features, arm and leg malformations, and genitourinary abnormalities.The FGFR2 gene mutations that cause these conditions ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
  8. FGFR3 gene 
    ... premature joining of the bones of the skull (craniosynostosis), leading to a misshapen head and distinctive facial features. It also causes a skin abnormality called acanthosis nigricans that is characterized by thick, ...
    https://medlineplus.gov/genetics/gene/fgfr3 - Genetics
  9. Apert syndrome 
    ... 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
  10. Osteoglophonic dysplasia 
    ... dysplasia depends on the extent of their craniofacial abnormalities; those that obstruct the air passages and affect the mouth and teeth can lead to respiratory problems and cause difficulty ...
    https://medlineplus.gov/genetics/condition/osteoglophonic-dysplasia - Genetics
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