Silver-Russell syndrome

Definition

Silver-Russell syndrome (SRS) is a disorder present at birth involving poor growth. One side of the body may also appear to be larger than the other.

Alternative Names

Russell-Silver syndrome; Silver syndrome; SRS

Causes

In 35% to 67% of cases, SRS is due to a variant in chromosome 11. A variant in chromosome 7 accounts for 7% to 10% of cases. The remaining 30% to 40% of cases have unknown causes.

Most of the time, it occurs in people with no family history of the disease.

The estimated number of people who develop this condition varies greatly. Males and females are equally affected.

Symptoms

Symptoms can include:

Exams and Tests

The condition is usually diagnosed by early childhood. Your health care provider will perform a physical exam.

There are no specific lab tests to diagnose SRS. The diagnosis is usually based on the judgment of your child's provider. 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 a person with this condition. They include:

Outlook (Prognosis)

Older children and adults do not show typical features as clearly as infants or younger children. Intelligence may be normal, although the person may have a learning disability. Birth defects of the urinary tract may be present.

Possible Complications

People with SRS may have these problems:

When to Contact a Medical Professional

Contact your child's provider if signs of SRS develop. Make sure your child's height and weight are measured during each well-child visit. Your provider may refer you to:

References

Senaratne TN, Zackai EH, Saitta SC. Chromosome disorders. In: Gleason CA, Sawyer T, eds. Avery's Diseases of the Newborn. 11th ed. Philadelphia, PA: Elsevier; 2024:chap 28.

Wakeling EL, Brioude F, Lokulo-Sodipe O, et al. Diagnosis and management of Silver-Russell syndrome: first international consensus statement. Nat Rev Endocrinol. 2017;13(2):105-124. PMID: 27585961 pubmed.ncbi.nlm.nih.gov/27585961/.



Review Date: 11/6/2024
Reviewed By: Anna C. Edens Hurst, MD, MS, Associate Professor in Medical Genetics, The University of Alabama at Birmingham, Birmingham, AL. Review provided by VeriMed Healthcare Network. Also reviewed by David C. Dugdale, MD, Medical Director, Brenda Conaway, Editorial Director, and the A.D.A.M. Editorial team. Editorial update 03/05/2025.
The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. No warranty of any kind, either expressed or implied, is made as to the accuracy, reliability, timeliness, or correctness of any translations made by a third-party service of the information provided herein into any other language. © 1997- A.D.A.M., a business unit of Ebix, Inc. Any duplication or distribution of the information contained herein is strictly prohibited.
© 1997- adam.comAll rights reserved.
A.D.A.M. content is best viewed in IE9 or above, Firefox and Google Chrome browser.