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Genetic and Rare Diseases Information Center (GARD)

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Orofaciodigital syndrome 4


Other Names for this Disease

  • Baraitser-Burn syndrome
  • OFD syndrome 4
  • OFD syndrome with tibial defects
  • OFD4
  • OFDS 4
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.

Overview

Orofaciodigital syndrome 4 is one of a group of related conditions that affect the development of the oral cavity (the mouth and teeth), facial features, and digits (fingers and toes).[1] Specific features, while variable, commonly include non-cancerous tumors (hamartomas) of the tongue, polydactyly of the hands and feet, severe clubfoot, and shortening and bowing of the middle portion of the lower leg (mesomelic limb shortening with tibial dysplasia). Orofaciodigital syndrome 4 is inherited in an autosomal recessive fashion.[2][3] The condition appears to be caused by mutations in the tectonic family member 3 gene (TCTN3).[3]
Last updated: 3/23/2013

References

  1. Oral-facial-digital syndrome. Genetics Home Reference (GHR). February 2010; http://ghr.nlm.nih.gov/condition/oral-facial-digital-syndrome. Accessed 3/23/2013.
  2. Vazquez MP. Oral-facial-digital syndrome type 4. Orphanet. November 2009; http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=2509. Accessed 3/23/2013.
  3. Orofaciodigital Syndrome IV. Online Mendelian Inheritance in Man (OMIM). September 2012; http://omim.org/entry/258860. Accessed 3/23/2013.
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Please contact us with your questions about Orofaciodigital syndrome 4. We will answer your question and update these pages with new resources and information.

Basic Information

  • Genetics Home Reference (GHR) contains information on Orofaciodigital syndrome 4. This website is maintained by the National Library of Medicine.
  • The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. Click on the link to view information on this topic.

In Depth Information

  • Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs.  Access to this database is free of charge.
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Orofaciodigital syndrome 4. Click on the link to view a sample search on this topic.
Other Names for this Disease
  • Baraitser-Burn syndrome
  • OFD syndrome 4
  • OFD syndrome with tibial defects
  • OFD4
  • OFDS 4
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.