A case report: Marfan syndrome with X trisomy and FBN1 and SDHB mutations
Abstract Background Marfan syndrome (MFS) is a rare autosomal dominant connective tissue disorder affecting the cardiovascular, skeletal, and ophthalmic systems. This report aimed to describe a novel genetic background and treatment prognosis of MFS. Case presentation A proband was initially diagnos...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
BMC,
2023-05-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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