Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 14 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. FGFR1 gene 
    ... show abnormal bone growth that leads to craniofacial abnormalities, including the premature fusion of certain bones in the skull (craniosynostosis). They may also lack teeth, or their teeth may not appear until later ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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
  9. Osteoglophonic dysplasia 
    ... the air passages and affect the mouth and teeth may have respiratory problems and difficulty eating and drinking. Despite the skull abnormalities, intelligence is generally not affected in people with ...
    https://medlineplus.gov/genetics/condition/osteoglophonic-dysplasia - Genetics
  10. 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
previous · 1 · 2 · next