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.

Related categories 2

GeneReviews: Russell-Silver Syndrome
Summary, diagnosis, clinical description, differential diagnosis, management, genetic counseling and molecular genetics.
NORD: Russell Silver Syndrome
Offers a general discussion, the synonyms and further resources.
Patient: Russell-Silver Syndrome
Factsheet on this inherited disorder, including its epidemiology, genetics, presentating features, differential diagnosis, investigations, management and prognosis.
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Last update:
March 9, 2016 at 19:54:10 UTC
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