Results 1 - 10 of 17 for Osteogenesis imperfecta type III
  1. Genetics Home Reference: Osteogenesis imperfecta From the National Institutes of Health (National Library of Medicine)  
    ... copy of the altered gene. Some cases of osteogenesis imperfecta type III are autosomal recessive; these cases usually result from ... Registry: Osteogenesis imperfecta type I Genetic Testing Registry: ... Genetic Testing Registry: Osteogenesis imperfecta with normal sclerae, ...
  2. Osteogenesis Imperfecta Issues: Constipation (Osteogenesis Imperfecta Foundation)  
    ... Rinsky LA. Gastrointestinal Problems in Patients Who Have Type III Osteogenesis Imperfecta. The Journal of Bone and Joint Surgery, 1995, ...
  3. Osteogenesis Imperfecta Glossary (Osteogenesis Imperfecta Foundation)  
    ... Sometimes referred to as the "moderate" form of osteogenesis imperfecta. It is in between Type I and Type III in severity. (For more information see the fact ...
  4. Genetics Home Reference: Dentinogenesis imperfecta From the National Institutes of Health (National Library of Medicine)  
    ... abnormalities. Type I occurs in people who have osteogenesis imperfecta, a genetic condition in which bones are brittle and easily broken. Dentinogenesis imperfecta type II and type III usually occur in people without other inherited disorders. ...
  5. Learning about Osteogenesis Imperfecta From the National Institutes of Health (National Human Genome Research Institute)  
    ... by the disorder. The autosomal recessive form of type III OI usually results from mutations in genes other than COL1A1 and COL1A2 . Top of page NHGRI Research on Osteogenesis imperfecta Currently, NHGRI is not conducting clinical research on ...
  6. Surgery Considerations for Adults and Children (Osteogenesis Imperfecta Foundation) - PDF  
    ... helping people cope with the problems associated with osteogenesis ... particularly those with OI Type III or those with short stature, may have compromised ...
  7. Types of OI (Osteogenesis Imperfecta Foundation)  
    ... VIII are similar to OI Types II or III in appearance and symptoms except for white ... 3-hydroxylase activity due to mutations in the LEPRE1 gene.
  8. Child Abuse or Osteogenesis Imperfecta? (Osteogenesis Imperfecta Foundation) - PDF  
    ... education, awareness, and mutual support. Clinical Features of Osteogenesis Imperfecta Type I (Mild) • Most common and mildest type of ... of these substances in the blood. The national Osteogenesis ... with all types of OI. Foundation staff can suggest appropriate professionals ...
  9. Rare Diseases and Related Terms From the National Institutes of Health (Office of Rare Diseases)  
    ... unilateral - See Adactylia unilateral * Adair-Dighton syndrome - See Osteogenesis imperfecta type 1 * ADAM syndrome - See Amniotic band syndrome * Adamantinoma - ...
  10. OI Issues: Dental Care for Persons with OI (Osteogenesis Imperfecta Foundation)  
    ... Imperfecta (DI) Dentinogenesis imperfecta can be part of osteogenesis imperfecta (DI type I) or it can be a separate inherited ...
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