Marfan Syndrome: A Case Report
Marfan syndrome is an autosomal dominant systemic disorder of the connective tissue. Children affected by the Marfan syndrome carry a mutation in one of their two copies of the gene that encodes the connective tissue protein fibrillin-1. Marfan syndrome affects most organs and tissues, especially th...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Hindawi Limited,
2012-01-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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