Russell-Silver Syndrome is a very rare genetic disorder characterized by growth delays before birth (prenatal or intrauterine growth retardation); overgrowth of one side of the body (hemihypertrophy or asymmetry); unusual characteristic facial features; and other physical abnormalities.
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- NORD: Russell Silver Syndrome Offers a general discussion, the synonyms and further resources.
- GeneReviews: Russell-Silver Syndrome Summary, diagnosis, clinical description, differential diagnosis, management, genetic counseling and molecular genetics.
- Patient: Russell-Silver Syndrome Factsheet on this inherited disorder, including its epidemiology, genetics, presentating features, differential diagnosis, investigations, management and prognosis.