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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...
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| 主要な著者: | , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Paediatrician Publishers, LLC
2015-08-01
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| シリーズ: | Pediatričeskaâ Farmakologiâ |
| 主題: | |
| オンライン･アクセス: | https://www.pedpharma.ru/jour/article/view/472 |
| タグ: |
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