ASSOCIATION OF BILATERAL RADIOULNAR SYNOSTOSIS WITH OSTEOGENESIS IMPERFECTA TYPE 1 - CASE PRESENTATION
Osteogenesis imperfecta (OI) is a group of rare congenital conditions characterized mainly by bone brittleness secondary to mutations in the genes encoding collagen. The medical history together with a clinical examination in detail of the fractures is highly important in directing the diagnosis tow...
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| Main Authors: | , , , , , , |
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| Format: | Book |
| Published: |
Romanian Society of Oral Rehabilitation,
2016-01-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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