29 May 2024 : Clinical Research
A Retrospective Study of the Presentation, Diagnosis, Management, and Outcomes of 27 Patients with Osteogenesis Imperfecta at a Single Center in Türkiye
Mehmet Yiğit Gökmen
1ABCDEF*, Akif Mirioğlu 2E, Buğra Kundakçı2E, İbrahim Boğa3BE, Ömer Sunkar Biçer2ACE
DOI: 10.12659/MSM.944364
Med Sci Monit 2024; 30:e944364
Table 1 Osteogenesis imperfecta classification according to the International Society of Skeletal Dysplasias.
| Osteogenesis imperfecta | Type | Inheritance/genes |
|---|---|---|
| Nondeforming | I | X-linked/PLS3 |
| Perinatal | II | |
| Progressively deforming | III | |
| Moderate | IV | |
| Calcification of interosseous membrane or hypertrophic callus | V | |
| AD – autosomal dominant; AR –autosomal recessive. | ||