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Genetics Home Reference: your guide to understanding genetic conditions
http://ghr.nlm.nih.gov/     A service of the U.S. National Library of Medicine®

Ring chromosome 14 syndrome

Reviewed May 2009

What is ring chromosome 14 syndrome?

Ring chromosome 14 syndrome is a condition characterized by seizures and intellectual disability. Recurrent seizures (epilepsy) develop in infancy or early childhood. In many cases, the seizures are resistant to treatment with anti-epileptic drugs. Most people with ring chromosome 14 syndrome also have some degree of intellectual disability or learning problems. Development may be delayed, particularly the development of speech and of motor skills such as sitting, standing, and walking.

Additional features of ring chromosome 14 syndrome can include slow growth and short stature, a small head (microcephaly), puffy hands and/or feet caused by a buildup of fluid (lymphedema), and subtle differences in facial features. Some affected individuals have problems with their immune system that lead to recurrent infections, especially involving the respiratory system. Abnormalities of the retina, the specialized tissue at the back of the eye that detects light and color, have also been reported in some people with this condition. These changes typically do not affect vision. Major birth defects are rarely seen with ring chromosome 14 syndrome.

How common is ring chromosome 14 syndrome?

Ring chromosome 14 syndrome appears to be a rare condition, although its prevalence is unknown. More than 50 affected individuals have been reported in the medical literature.

What are the genetic changes related to ring chromosome 14 syndrome?

Ring chromosome 14 syndrome is caused by a chromosomal abnormality known as a ring chromosome 14 or r(14). A ring chromosome is a circular structure that occurs when a chromosome breaks in two places and its broken ends fuse together. People with ring chromosome 14 syndrome have one copy of this abnormal chromosome in some or all of their cells.

Researchers believe that several critical genes near the end of the long (q) arm of chromosome 14 are lost when the ring chromosome forms. The loss of these genes is likely responsible for several of the major features of ring chromosome 14 syndrome, including intellectual disability and delayed development. Researchers are still working to determine which missing genes contribute to the signs and symptoms of this disorder.

Epilepsy is a common feature of ring chromosome syndromes, including ring chromosome 14. There may be something about the ring structure itself that causes epilepsy. Seizures may occur because certain genes on the ring chromosome 14 are less active than those on the normal chromosome 14. Alternately, seizures might result from instability of the ring chromosome in some cells.

Related Chromosome(s)

Changes involving this chromosome are associated with ring chromosome 14 syndrome.

  • chromosome 14

Can ring chromosome 14 syndrome be inherited?

Ring chromosome 14 syndrome is almost never inherited. A ring chromosome typically occurs as a random event during the formation of reproductive cells (eggs or sperm) or in early embryonic development. In some cases, the ring chromosome is present in only some of a person's cells. This situation is known as mosaicism.

Most affected individuals have no history of the disorder in their families. However, at least two families have been reported in which a ring chromosome 14 was passed from a mother to her children.

Where can I find information about diagnosis or management of ring chromosome 14 syndrome?

These resources address the diagnosis or management of ring chromosome 14 syndrome and may include treatment providers.

  • Genetic Testing Registry: Ring chromosome 14 (http://www.ncbi.nlm.nih.gov/gtr/conditions/C2930916)
  • MedlinePlus Encyclopedia: Chromosome (http://www.nlm.nih.gov/medlineplus/ency/article/002327.htm)

You might also find information on the diagnosis or management of ring chromosome 14 syndrome in Educational resources (http://www.ghr.nlm.nih.gov/condition/ring-chromosome-14-syndrome/show/Educational+resources) and Patient support (http://www.ghr.nlm.nih.gov/condition/ring-chromosome-14-syndrome/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 ring chromosome 14 syndrome?

You may find the following resources about ring chromosome 14 syndrome 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 ring chromosome 14 syndrome?

  • ring 14
  • ring 14 syndrome
  • ring chromosome 14

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 ring chromosome 14 syndrome?

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

What glossary definitions help with understanding ring chromosome 14 syndrome?

chromosome ; disability ; embryonic ; epilepsy ; epileptic ; immune system ; inherited ; lymphedema ; microcephaly ; mosaicism ; motor ; prevalence ; reproductive cells ; respiratory ; retina ; short stature ; somatic mosaicism ; sperm ; stature ; syndrome ; telomere ; 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

  • Lippe BM, Sparkes RS. Ring 14 chromosome: association with seizures. Am J Med Genet. 1981;9(4):301-5. (http://www.ncbi.nlm.nih.gov/pubmed/6170224?dopt=Abstract)
  • Matalon R, Supple P, Wyandt H, Rosenthal IM. Transmission of ring 14 chromosome from mother to two sons. Am J Med Genet. 1990 Aug;36(4):381-5. Review. (http://www.ncbi.nlm.nih.gov/pubmed/2202211?dopt=Abstract)
  • Morimoto M, Usuku T, Tanaka M, Otabe O, Nishimura A, Ochi M, Takeuchi Y, Yoshioka H, Sugimoto T. Ring chromosome 14 with localization-related epilepsy: three cases. Epilepsia. 2003 Sep;44(9):1245-9. (http://www.ncbi.nlm.nih.gov/pubmed/12919399?dopt=Abstract)
  • Riley SB, Buckton KE, Ratcliffe SG, Syme J. Inheritance of a ring 14 chromosome. J Med Genet. 1981 Jun;18(3):209-13. (http://www.ncbi.nlm.nih.gov/pubmed/7241544?dopt=Abstract)
  • Schlade-Bartusiak K, Costa T, Summers AM, Nowaczyk MJ, Cox DW. FISH-mapping of telomeric 14q32 deletions: search for the cause of seizures. Am J Med Genet A. 2005 Oct 15;138A(3):218-24. (http://www.ncbi.nlm.nih.gov/pubmed/16152642?dopt=Abstract)
  • Unique support group booklet about ring chromosome 14 (http://www.rarechromo.org/information/Chromosome%2014/Ring%2014%20FTNW.pdf)
  • van Karnebeek CD, Quik S, Sluijter S, Hulsbeek MM, Hoovers JM, Hennekam RC. Further delineation of the chromosome 14q terminal deletion syndrome. Am J Med Genet. 2002 Jun 1;110(1):65-72. Review. (http://www.ncbi.nlm.nih.gov/pubmed/12116274?dopt=Abstract)
  • Wintle RF, Costa T, Haslam RH, Teshima IE, Cox DW. Molecular analysis redefines three human chromosome 14 deletions. Hum Genet. 1995 May;95(5):495-500. (http://www.ncbi.nlm.nih.gov/pubmed/7759068?dopt=Abstract)
  • Zelante L, Torricelli F, Calvano S, Mingarelli R, Dallapiccola B. Ring chromosome 14 syndrome. Report of two cases, including extended evaluation of a previously reported patient and review. Ann Genet. 1991;34(2):93-7. Review. (http://www.ncbi.nlm.nih.gov/pubmed/1746891?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 2009
Published: October 20, 2014