Syndactyly type 3
Other Names for this Disease
- Syndactyly of the ring and little finger
- Syndactyly of fingers four and five
- Ring and little finger syndactyly
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Syndactyly type 3 has been shown to be inherited in an autosomal dominant manner. This means that having only one mutated copy of the causative gene is sufficient to cause the condition. When an individual with an autosomal dominant condition has children, each child has a 50% (1 in 2) chance of inheriting the mutated gene and a 50% chance of inheriting the normal gene and being unaffected.
Last updated: 6/3/2013
- Syndactyly type 3. Orphanet. October 2010; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=93404. Accessed 6/3/2013.