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Results 1 - 10 of 14 for Premature loss of teeth
  1. Hypophosphatasia 
    ... this disorder typically experience abnormal tooth development and premature tooth loss, but do not have the skeletal abnormalities seen ...
    https://medlineplus.gov/genetics/condition/hypophosphatasia - Genetics
  2. Mandibuloacral dysplasia 
    ... Some people with this condition have features of premature aging (a condition called progeria), such as thin skin, loss of teeth, loss of hair, and a beaked nose. Some ...
    https://medlineplus.gov/genetics/condition/mandibuloacral-dysplasia - Genetics
  3. FGFR2 gene 
    ... overactivate signaling by the FGFR2 protein, which promotes premature fusion of ... saliva production, small teeth, and hand deformities. A mutation that occurs in ...
    https://medlineplus.gov/genetics/gene/fgfr2 - Genetics
  4. Carpenter syndrome 
    Carpenter syndrome is a condition characterized by the premature fusion of certain skull bones (craniosynostosis), abnormalities of ... to increased pressure within the skull (intracranial pressure). Premature fusion of the skull bones can cause several ...
    https://medlineplus.gov/genetics/condition/carpenter-syndrome - Genetics
  5. Branchio-oculo-facial syndrome 
    ... characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature aging Hemangiomatous branchial clefts-lip pseudocleft syndrome Lip ...
    https://medlineplus.gov/.../condition/branchio-oculo-facial-syndrome - Genetics
  6. Apert syndrome 
    ... A key feature of Apert syndrome is the premature closure of the bones of the skull (craniosynostosis). ... of the characteristic facial features of Apert syndrome. Premature fusion of the skull bones prevents the head ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  7. FGFR1 gene 
    ... the olfactory bulb. In addition, the misplacement or premature loss of GnRH-producing neurons prevents the production ... growth that leads to craniofacial abnormalities, including the premature fusion of certain bones in the skull (craniosynostosis). ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics
  8. FGFR3 gene 
    ... syndrome with acanthosis nigricans. This rare condition causes premature joining of the bones of the skull (craniosynostosis), ... coronal craniosynostosis. This condition is characterized by a premature fusion of the growth line that runs across ...
    https://medlineplus.gov/genetics/gene/fgfr3 - Genetics
  9. Short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay 
    ... older than their biological age. This appearance of premature aging is sometimes described as progeroid.Most people ... increased pressure in the eye (glaucoma) and vision loss. Some people with SHORT ... (eruption) of teeth in early childhood, small teeth, fewer teeth than ...
    https://medlineplus.gov/...ression-rieger-anomaly-and-teething-delay - Genetics
  10. LAMA3 gene 
    ... 332. Most of these mutations lead to a premature stop signal in the instructions for making all ... body can lead to serious complications, including vision loss and blockage of ... nails and abnormal teeth.The mutations involved in LOC syndrome lead to ...
    https://medlineplus.gov/genetics/gene/lama3 - Genetics
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