Unveiling the uncommon: diagnostic journey of camurati-engelmann disease in a pediatric patient
Abstract Background Camurati-Engelmann disease (CED), also known as progressive diaphyseal dysplasia, is a rare genetic disorder characterized by abnormal thickening of the long bones' diaphysis. This condition is caused by mutations in the transforming growth factor beta-1 (TGFB-1) gene and is...
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| Main Authors: | , , , |
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| Format: | Book |
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BMC,
2024-10-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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