There is no one cause known for this rare disorder. Most cases are sporadic, that is, occur as an isolated finding in a family with no other affected family member. The features associated with Russell-Silver syndrome have been described in association with many genetic abnormalities such as: - chromosome rearrangements
- uniparental disomy (UPD) 7
- autosomal dominant and recessive families (rarely reported)
More than 400 cases have been reported. Estimates of incidence range from as high as 1 in 3,000 to as low as 1 in 100,000. Males and females are equally affected.
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