PedAM
Pediatric Disease Annotations & Medicines
| Disease | osteogenesis imperfecta |
| Symptom | C0011436|dentinogenesis imperfecta |
| Sentences | 7 |
| PubMedID- 21291557 | Dgi type i is osteogenesis imperfecta with dentinogenesis imperfecta and is caused by mutations in col1a1 and col1a2 7. |
| PubMedID- 25578972 | Immunohistochemical analysis was used to assay type i and vi collagen, various non-collagenous proteins distribution in human primary teeth from healthy patients or from patients affected by type i dentinogenesis imperfecta (dgi-i) associated with osteogenesis imperfecta (oi). |
| PubMedID- 24371383 | dentinogenesis imperfecta (di) associated with osteogenesis imperfecta (oi) is a genetic disorder that affects the connective tissues and results in dentine dysplasia. |
| PubMedID- 23802117 | Earlier studies had reported the presence of widened and infected pulp cavities characteristic of dentinogenesis imperfecta in patients with osteogenesis imperfecta 7. |
| PubMedID- 20384825 | dentinogenesis imperfecta in children with osteogenesis imperfecta: a clinical and ultrastructural study. |
| PubMedID- 23162594 | dentinogenesis imperfecta associated with osteogenesis imperfecta. |
| PubMedID- 23579912 | osteogenesis imperfecta/lobstein syndrome associated with dentinogenesis imperfecta. |
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