Growth Delay, Constitutional

National Organization for Rare Disorders, Inc.

Important
It is possible that the main title of the report Growth Delay, Constitutional is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.

Synonyms

  • Constitutional Delay in Growth and Puberty
  • Constitutional Short Stature
  • Idiopathic Growth Delay
  • Physiologic Delayed Puberty
  • Sporadic Short Stature
  • CDGP
  • CGD
  • Constitutional Delay in Growth and Adolescence

Disorder Subdivisions

  • None

General Discussion

Constitutional growth delay (CGD) is a term describing a temporary delay in the skeletal growth and height of a child with no other physical abnormalities causing the delay. Short stature may be the result of a growth pattern inherited from a parent (familial) or occur for no apparent reason (idiopathic). Typically at some point during childhood growth slows down, eventually resuming at a normal rate. CGD is the most common cause of short stature and delayed puberty. The exact cause of CGD is unknown.
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Resources

Human Growth Foundation
997 Glen Cove Avenue
Glen Head, NY 11545
Tel: (516)671-4041
Fax: (516)671-4055
Tel: (800)451-6434
Email: hgf1@hgfound.org
Internet: http://www.hgfound.org/

MAGIC Foundation
6645 W. North Avenue
Oak Park, IL 60302
Tel: (708)383-0808
Fax: (708)383-0899
Tel: (800)362-4423
Email: mary@magicfoundation.org
Internet: http://www.magicfoundation.org

Little People's Research Fund, Inc.
616 Old Edmondson Avenue
2nd Floor
Catonsville, MD 21228-3305
USA
Tel: (410)747-1100
Fax: (410)747-1374
Tel: (800)232-5773
Email: lprf@lprf.org
Internet: http://www.lprf.org

Little People of America, Inc.
250 El Camino Real
Suite 201
Tustin, CA 92780
Tel: (714)368-3689
Fax: (714)368-3367
Tel: (888)572-2001
Email: info@lpaonline.org
Internet: http://www.lpaonline.org

For a Complete Report

For a Complete Report

This is an abstract of a report from the National Organization for Rare Disorders, Inc. ® (NORD). A copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html

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