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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mutations in the GJA1 gene, which has also been implicated in a condition called oculodentodigital dysplasia. SD3 is the characteristic digital abnormality in this condition. SD3 is inherited in an autosomal dominant manner.Syndactyly type 3 (SD3) is a limb abnormality present at birth that is characterized by complete fusion of the 4th and 5th fingers on both hands. In most cases only the soft tissue is fused, but in some cases the bones of the fingers (distal phalanges) are fused. There is evidence that SD3 is caused by
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.
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- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
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