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Results 1 - 10 of 38 for Premature loss of teeth
  1. Hypophosphatasia (Osteogenesis Imperfecta Foundation) - PDF  
    Osteogenesis Imperfecta/Related Issues ... Osteogenesis Imperfecta ... Bone Diseases/Specifics ... Bone Diseases ... Osteogenesis Imperfecta Foundation ... PDF
    https://oif.org/wp-content/uploads/2019/10/hypophosphatasia-2.pdf - External Health Links
  2. 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
  3. 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
  4. 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
  5. Caring for Your Premature Baby (American Academy of Family Physicians)  
    Premature Babies/Living With ... Premature Babies ... American Academy of Family Physicians
    https://familydoctor.org/caring-for-your-premature-baby/?adfree=true - External Health Links
  6. 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
  7. 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
  8. Easy-to-Read Health Information 
    ... and Digestive and Kidney Diseases) Also in Spanish Premature Babies Necrotizing Enterocolitis (NEC) (Eunice Kennedy Shriver National ...
    https://medlineplus.gov/all_easytoread.html -
  9. 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
  10. 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
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