What is the treatment for Russell-Silver syndrome?

What is the treatment for Russell-Silver syndrome?

Treatment for RSS focuses on treating its symptoms so the child can develop as normally as possible. Treatments to help with growth and development include: a nutrition schedule with specified snack and meal times. growth hormone injections.

Is Russell-Silver syndrome a disability?

LP’s history and test findings yielded a profile consistent with a nonverbal learning disability, with significantly higher verbal compared to nonverbal intelligence, deficient visual-spatial memory, fine motor coordination and motor planning problems, relatively greater difficulty in math compared to other achievement …

Can people with Russell-Silver syndrome have children?

An adult female with typical features of Silver-Russell dwarfism gave birth to a viable infant. Despite the abnormalities in sexual development that may be associated with the Silver-Russell syndrome, fertility is not necessarily impaired, at least in females.

How do you know if your child has Russell-Silver syndrome?

Russell-Silver syndrome (RSS) is a rare condition associated with poor growth both before and after birth. Signs and symptoms vary and may include low birth weight, short stature , characteristic facial features, large head in relation to body size, body asymmetry, and feeding difficulties.

How tall are people with Russell-Silver syndrome?

Adults with Russell-Silver syndrome are short; the average height for affected men is about 151 centimeters (4 feet, 11 inches) and the average height for affected women is about 140 centimeters (4 feet, 7 inches).

Which is a characteristic of Russell-Silver syndrome?

Summary. Russell-Silver syndrome (RSS) is a rare disorder characterized by intrauterine growth restriction (IUGR), poor growth after birth, a relatively large head size, a triangular facial appearance, a prominent forehead (looking from the side of the face), body asymmetry and significant feeding difficulties.

How long do people with Russell-Silver syndrome live?

With appropriate medical care, most individuals with RSS will live full, productive lives. Growth and puberty: Almost all infants with RSS have a birth weight well below the 3rd percentile (<-2SD) even at full term.

How do you test for Russell-Silver syndrome?

HOW IS RUSSELL-SILVER SYNDROME DIAGNOSED? Molecular Testing: Russell-Silver syndrome can be diagnosed with genetic testing; but negative genetic testing does not rule out a clinical diagnosis. Currently, genetic testing can be run for known causes of Russell-Silver Syndrome involving chromosomes 7 and 11.

How do people get Russell-Silver syndrome?

Rarely, Russell-Silver syndrome can run in families. In some affected families, the condition appears to have an autosomal dominant pattern of inheritance. Autosomal dominant inheritance means one copy of a genetic change in each cell is sufficient to cause the disorder.

Is Russell-Silver syndrome rare?

Russell-Silver syndrome (RSS) is a rare disorder characterized by intrauterine growth restriction (IUGR), poor growth after birth, a relatively large head size, a triangular facial appearance, a prominent forehead (looking from the side of the face), body asymmetry and significant feeding difficulties.

Is Russell-Silver syndrome a genetic disorder?

Russell-Silver syndrome (RSS) is a genetic disorder that usually results from the abnormal regulation of certain genes that control growth.