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Russell-Silver syndrome

Definition

Russell-Silver syndrome is a disorder present at birth that involves poor growth, low birth weight, short height, and differences in the size of the two sides of the body.

Alternative Names

Silver-Russell syndrome; Silver syndrome

Causes, incidence, and risk factors

An estimated 7 - 10% of patients with this syndrome have a defect in a gene called the maternal uniparental disomy (UPD) for chromosome 7. However, a cause cannot be identified in most patients. Most cases occur in people with no family history of the disease.

The estimated number of people who develop this condition varies greatly. Some say it affects about 1 in 3,000 people. Other reports say it affects 1 in 100,000 people. Males and females are equally affected.

Symptoms

Signs and tests

The condition is usually diagnosed by early childhood. The doctor will perform a physical exam. Signs include:

  • Small, pointed chin
  • Thin, wide mouth
  • Triangle-shaped face with broad forehead

There are no specific laboratory tests to diagnose Russell-Silver syndrome. However, the following tests may be done:

Treatment

Growth hormone replacement may help if this hormone is lacking. Other treatments include:

Many specialists may be involved in treating this condition:

  • A doctor specializing in genetics can help diagnose Russell-Silver syndrome.
  • A gastroenterologist or nutritionist can help develop the proper diet to enhance growth.
  • An endocrinologist may prescribe growth hormone, if it is needed.
  • Genetic counselors and psychologists may also be involved.

Expectations (prognosis)

Older children and adults do not show typical features as clearly as infants or younger children. Intelligence may be normal, although the patient may have a learning disability.

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