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Genetics Home Reference: your guide to understanding genetic conditions
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Achondroplasia

Reviewed May 2012

What is achondroplasia?

Achondroplasia is a form of short-limbed dwarfism. The word achondroplasia literally means "without cartilage formation." Cartilage is a tough but flexible tissue that makes up much of the skeleton during early development. However, in achondroplasia the problem is not in forming cartilage but in converting it to bone (a process called ossification), particularly in the long bones of the arms and legs. Achondroplasia is similar to another skeletal disorder called hypochondroplasia, but the features of achondroplasia tend to be more severe.

All people with achondroplasia have short stature. The average height of an adult male with achondroplasia is 131 centimeters (4 feet, 4 inches), and the average height for adult females is 124 centimeters (4 feet, 1 inch). Characteristic features of achondroplasia include an average-size trunk, short arms and legs with particularly short upper arms and thighs, limited range of motion at the elbows, and an enlarged head (macrocephaly) with a prominent forehead. Fingers are typically short and the ring finger and middle finger may diverge, giving the hand a three-pronged (trident) appearance. People with achondroplasia are generally of normal intelligence.

Health problems commonly associated with achondroplasia include episodes in which breathing slows or stops for short periods (apnea), obesity, and recurrent ear infections. In childhood, individuals with the condition usually develop a pronounced and permanent sway of the lower back (lordosis) and bowed legs. Some affected people also develop abnormal front-to-back curvature of the spine (kyphosis) and back pain. A potentially serious complication of achondroplasia is spinal stenosis, which is a narrowing of the spinal canal that can pinch (compress) the upper part of the spinal cord. Spinal stenosis is associated with pain, tingling, and weakness in the legs that can cause difficulty with walking. Another uncommon but serious complication of achondroplasia is hydrocephalus, which is a buildup of fluid in the brain in affected children that can lead to increased head size and related brain abnormalities.

How common is achondroplasia?

Achondroplasia is the most common type of short-limbed dwarfism. The condition occurs in 1 in 15,000 to 40,000 newborns.

What genes are related to achondroplasia?

Mutations in the FGFR3 gene cause achondroplasia. The FGFR3 gene provides instructions for making a protein that is involved in the development and maintenance of bone and brain tissue. Two specific mutations in the FGFR3 gene are responsible for almost all cases of achondroplasia. Researchers believe that these mutations cause the FGFR3 protein to be overly active, which interferes with skeletal development and leads to the disturbances in bone growth seen with this disorder.

Related Gene(s)

Changes in this gene are associated with achondroplasia.

  • FGFR3

How do people inherit achondroplasia?

Achondroplasia is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. About 80 percent of people with achondroplasia have average-size parents; these cases result from new mutations in the FGFR3 gene. In the remaining cases, people with achondroplasia have inherited an altered FGFR3 gene from one or two affected parents. Individuals who inherit two altered copies of this gene typically have a severe form of achondroplasia that causes extreme shortening of the bones and an underdeveloped rib cage. These individuals are usually stillborn or die shortly after birth from respiratory failure.

Where can I find information about diagnosis or management of achondroplasia?

These resources address the diagnosis or management of achondroplasia and may include treatment providers.

  • GeneFacts: Achondroplasia: Diagnosis (http://genefacts.org/index.php?option=com_content&view=article&id=470&Itemid=639)
  • GeneFacts: Achondroplasia: Management (http://genefacts.org/index.php?option=com_content&view=article&id=471&Itemid=640)
  • Gene Review: Achondroplasia (http://www.ncbi.nlm.nih.gov/books/NBK1152/)
  • Genetic Testing Registry: Achondroplasia (http://www.ncbi.nlm.nih.gov/gtr/conditions/C0001080)
  • MedlinePlus Encyclopedia: Achondroplasia (http://www.nlm.nih.gov/medlineplus/ency/article/001577.htm)
  • MedlinePlus Encyclopedia: Hydrocephalus (http://www.nlm.nih.gov/medlineplus/ency/article/001571.htm)
  • MedlinePlus Encyclopedia: Lordosis (http://www.nlm.nih.gov/medlineplus/ency/article/003278.htm)
  • MedlinePlus Encyclopedia: Spinal Stenosis (http://www.nlm.nih.gov/medlineplus/ency/article/000441.htm)

You might also find information on the diagnosis or management of achondroplasia in Educational resources (http://www.ghr.nlm.nih.gov/condition/achondroplasia/show/Educational+resources) and Patient support (http://www.ghr.nlm.nih.gov/condition/achondroplasia/show/Patient+support).

General information about the diagnosis (http://ghr.nlm.nih.gov/handbook/consult/diagnosis) and management (http://ghr.nlm.nih.gov/handbook/consult/treatment) of genetic conditions is available in the Handbook. Read more about genetic testing (http://ghr.nlm.nih.gov/handbook/testing), particularly the difference between clinical tests and research tests (http://ghr.nlm.nih.gov/handbook/testing/researchtesting).

To locate a healthcare provider, see How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.

Where can I find additional information about achondroplasia?

You may find the following resources about achondroplasia helpful. These materials are written for the general public.

You may also be interested in these resources, which are designed for healthcare professionals and researchers.

What other names do people use for achondroplasia?

  • ACH
  • achondroplastic dwarfism
  • dwarf, achondroplastic

For more information about naming genetic conditions, see the Genetics Home Reference Condition Naming Guidelines (http://ghr.nlm.nih.gov/ConditionNameGuide) and How are genetic conditions and genes named? (http://ghr.nlm.nih.gov/handbook/mutationsanddisorders/naming) in the Handbook.

What if I still have specific questions about achondroplasia?

Ask the Genetic and Rare Diseases Information Center (http://rarediseases.info.nih.gov/GARD/).

What glossary definitions help with understanding achondroplasia?

apnea ; autosomal ; autosomal dominant ; cartilage ; cell ; complication ; dwarf ; dwarfism ; gene ; hydrocephalus ; lordosis ; macrocephaly ; ossification ; protein ; respiratory ; short stature ; stature ; stenosis ; tissue

You may find definitions for these and many other terms in the Genetics Home Reference Glossary (http://www.ghr.nlm.nih.gov/glossary).

References

  • Gene Review: Achondroplasia (http://www.ncbi.nlm.nih.gov/books/NBK1152/)
  • Horton WA, Hall JG, Hecht JT. Achondroplasia. Lancet. 2007 Jul 14;370(9582):162-72. Review. (http://www.ncbi.nlm.nih.gov/pubmed/17630040?dopt=Abstract)
  • Horton WA, Lunstrum GP. Fibroblast growth factor receptor 3 mutations in achondroplasia and related forms of dwarfism. Rev Endocr Metab Disord. 2002 Dec;3(4):381-5. Review. (http://www.ncbi.nlm.nih.gov/pubmed/12424440?dopt=Abstract)
  • Horton WA. Recent milestones in achondroplasia research. Am J Med Genet A. 2006 Jan 15;140(2):166-9. (http://www.ncbi.nlm.nih.gov/pubmed/16353253?dopt=Abstract)
  • Laederich MB, Horton WA. Achondroplasia: pathogenesis and implications for future treatment. Curr Opin Pediatr. 2010 Aug;22(4):516-23. doi: 10.1097/MOP.0b013e32833b7a69. Review. (http://www.ncbi.nlm.nih.gov/pubmed/20601886?dopt=Abstract)
  • Trotter TL, Hall JG; American Academy of Pediatrics Committee on Genetics. Health supervision for children with achondroplasia. Pediatrics. 2005 Sep;116(3):771-83. Erratum in: Pediatrics. 2005 Dec;116(6):1615. (http://www.ncbi.nlm.nih.gov/pubmed/16140722?dopt=Abstract)
  • Vajo Z, Francomano CA, Wilkin DJ. The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans. Endocr Rev. 2000 Feb;21(1):23-39. Review. (http://www.ncbi.nlm.nih.gov/pubmed/10696568?dopt=Abstract)
  • Wright MJ, Irving MD. Clinical management of achondroplasia. Arch Dis Child. 2012 Feb;97(2):129-34. doi: 10.1136/adc.2010.189092. Epub 2011 Apr 3. Review. (http://www.ncbi.nlm.nih.gov/pubmed/21460402?dopt=Abstract)

 

The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? (http://ghr.nlm.nih.gov/handbook/consult/findingprofessional) in the Handbook.

 
Reviewed: May 2012
Published: July 7, 2014