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CLINICAL CASE OF RARE TYPE V OSTEOGENESIS IMPERFECTA
Osteogenesis imperfecta, also known as the brittle bone disease, is a clinically heterogenic hereditary connective tissue disease characterized by brittle bones and high risk of skeletal bone fractures. Other observable symptoms, such as deformities of limb and spinal bones, blue sclerae, dentinogen...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Paediatrician Publishers, LLC
2015-08-01
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| Σειρά: | Pediatričeskaâ Farmakologiâ |
| Θέματα: | |
| Διαθέσιμο Online: | https://www.pedpharma.ru/jour/article/view/472 |
| Ετικέτες: |
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