Type I osteogenesis imperfecta: a case report
The term osteogenesis imperfecta includes several genetic defects of type I collagen, clinically traduced in bone fragility and deformity. The type I or Lobstein variety is the most frequent form of the disease and is characterized by a pattern of autosomal dominant inheritance. The case of a 65-ye...
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| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
Universidad de Ciencias Médicas de Holguín
2022-02-01
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| Series: | Correo Científico Médico |
| Online Access: | https://revcocmed.sld.cu/index.php/cocmed/article/view/3955 |
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