A novel Noonan syndrome RAF1 mutation: lethal course in a preterm infant
Noonan syndrome is a relatively common and heterogeneous genetic disorder, associated with congenital heart defect in about 50% of the cases. If the defect is not severe, life expectancy is normal. We report a case of Noonan syndrome in a preterm infant with hypertrophic cardiomyopathy and lethal ou...
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| Main Authors: | , , , , , , , , , |
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| Format: | Book |
| Published: |
MDPI AG,
2015-06-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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