Saethre Chotzen syndrome

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autosomal dominant trait, craniosynostosis, syndrome

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• Saethre Chotzen Syndrome Important It is possible that the main title of the report Saethre Chotzen Syndrome is not the name you expected.
• Increased risk for developmental delay in Saethre-Chotzen syndrome is associated with TWIST deletions: an improved strategy for TWIST mutation screening.
• Saethre-Chotzen syndrome is an autosomal dominant disorder that affects between 1 and 2 in every 50,000 people.
• Saethre-Chotzen syndrome is an autosomal dominant disorder that affects between 1 and 2 in every 50,000 people.
• These results provide further evidence that the genetic locus for Saethre-Chotzen syndrome is located in distal 7p.

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