A CLINICAL CASE OF OSTEOGENESIS IMPERFECT TYPE III, DETERMINED BY COL1A1 (P.GLY845ARG) GENE MUTATION IN A NEWBORN GIRL
Osteogenesis imperfecta (OI) is a disease that is characterized by hereditary connective tissue dysplasia and is clinically manifested as excessive bone fragility and limb deformity. The overall incidence of OI is 1:10,000-20,000 live births. The main autosomal dominant inheritance path, autosomal r...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
Bukovynian State Medical University,
2022-05-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |