The National Organization for Rare Disorders (NORD)

Database Subscriptions

Many libraries, schools, universities, and hospitals subscribe to NORD’s Rare Disease Database for unlimited access to reports on more than 1,200 diseases.

Index of Rare Diseases

This is the list of diseases currently covered in the Rare Disease Database.

Rare Disease Database

Search this database for reports on more than 1,200 diseases.

View sample report

Index of Organizations

This is the list of organizations in NORD’s Organizational Database.

Organizational Database

Read about more than 2,000 patient organizations and other sources of help.

NORD's
Washington Office

NORD's Washington OfficeRead about events on Capitol Hill, funding for rare-disease research, and other topics of interest from NORD's office in Washington, DC.

 



Russell Silver Syndrome (RSS)

To purchase full-text report ($7.50):
View Cart/Checkout

The National Organization for Rare Disorders (NORD) web site, its databases, and the contents thereof are copyrighted by NORD. No part of the NORD web site, databases, or the contents may be copied in any way, including but not limited to the following: electronically downloading, storing in a retrieval system, or redistributing for any commercial purposes without the express written permission of NORD. Permission is hereby granted to print one hard copy of the information on an individual disease for your personal use, provided that such content is in no way modified, and the credit for the source (NORD) and NORD’s copyright notice are included on the printed copy. Any other electronic reproduction or other printed versions is strictly prohibited.

The information in NORD's Rare Disease Database is for educational purposes only. It should never be used for diagnostic or treatment purposes. If you have questions regarding a medical condition, always seek the advice of your physician or other qualified health professional. NORD's reports provide a brief overview of rare diseases. For more specific information, we encourage you to contact your personal physician or the agencies listed as "Resources" on this report.

Copyright 1987, 1990, 1997, 1999, 2003, 2007



Synonyms of Russell Silver Syndrome (RSS)
  • RSS
  • Russell-Silver Dwarfism
  • Russell Syndrome
  • Silver-Russell Dwarfism
  • Silver-Russell Syndrome
  • Silver Syndrome
  • SRS

Disorder Subdivisions

  • Russell-Silver Syndrome, X-linked (Partington Syndrome)


General Discussion
Russell-Silver syndrome (RSS) is a rare genetic disorder characterized by a wide variety of symptoms. RSS is genetically heterogeneous, meaning that different genetic abnormalities are believed to cause the disorder. RSS is characterized by a wide spectrum of symptoms and physical findings that vary in range and severity from case to case. The characteristic findings are growth delays before birth (prenatal or intrauterine growth retardation) and after birth (postnatal growth deficiency). Growth deficiency often results in short stature in adulthood. Additional common symptoms include unusual, distinctive facial features, a pinky that is fixed or 'locked' in a bent position (clinodactyly), and undergrowth of one side or structure of the body (hemihypotrophy), resulting in unequal (asymmetric) growth. Many children with RSS have normal intelligence, but rowing evidence suggests that there is an increased risk of learning disabilities. In most cases, the exact underlying genetic cause of RSS is not known.
.

Organizations related to Russell Silver Syndrome (RSS)
  • Arc
    1660 L Street, NW, Suite 301
    Washington DC 20036
    Phone #: 202-534-3700
    800 #: 800-433-5255
    e-mail: info@thearc.org
    Home page: http://www.thearc.org
  • Genetic and Rare Diseases (GARD) Information Center
    PO Box 8126
    Gaithersburg MD 20898-8126
    Phone #: 301-251-4925
    800 #: 888-205-2311
    e-mail: http://rarediseases.info.nih.gov/GARD/EmailForm.aspx
    Home page: http://rarediseases.info.nih.gov/GARD
  • Human Growth Foundation
    997 Glen Cove Avenue
    Glen Head NY 11545
    Phone #: 516-671-4041
    800 #: 800-451-6434
    e-mail: hgf1@hgfound.org
    Home page: http://www.hgfound.org/
  • Little People of America, Inc.
    250 El Camino Real
    Suite 201
    Tustin CA 92780
    Phone #: 714-368-3689
    800 #: 888-572-2001
    e-mail: info@lpaonline.org
    Home page: http://www.lpaonline.org
  • MAGIC Foundation
    6645 W. North Avenue
    Oak Park IL 60302
    Phone #: 708-383-0808
    800 #: 800-362-4423
    e-mail: mary@magicfoundation.org
    Home page: http://www.magicfoundation.org
  • MUMS National Parent-to-Parent Network
    150 Custer Court
    Green Bay WI 54301-1243
    Phone #: 920-336-5333
    800 #: 877-336-5333
    e-mail: mums@netnet.net
    Home page: http://www.netnet.net/mums/
  • Madisons Foundation
    PO Box 241956
    Los Angeles CA 90024
    Phone #: 310-264-0826
    800 #: N/A
    e-mail: getinfo@madisonsfoundation.org
    Home page: http://www.madisonsfoundation.org
  • NIH/National Arthritis and Musculoskeletal and Skin Diseases Information Clearinghouse
    1 AMS Circle
    Bethesda MD 20892-3675
    Phone #: 301-495-4484
    800 #: 877-226-4267
    e-mail: NIAMSinfo@mail.nih.gov
    Home page: http://www.niams.nih.gov/Health_Info
  • Restricted Growth Association
    PO Box 1024
    Peterborough Intl PE1 9GX
    Phone #: 030-0 1-11 1970
    800 #: --
    e-mail: office@restrictedgrowth.co.uk
    Home page: http://www.restrictedgrowth.co.uk

ABOUT NORD .|. CONTACT NORD .|. MEMBERSHIP .|. PRIVACY POLICY .|. DISCLAIMER .|. HOME
©2009 NORD - National Organization for Rare Disorders, Inc. All rights reserved.

Last modified Wednesday, November 26, 2008