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Genetic and Rare Diseases Information Center (GARD)

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Polydactyly myopia syndrome


Other Names for this Disease

  • Czeizel Brooser syndrome
  • PMS
  • Postaxial Polydactyly with progressive myopia
  • Postaxial polydactyly-progressive myopia syndrome
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Overview

Polydactyly myopia syndrome is characterized by postaxial polydactyly (the presence of an extra digit on the side of the hand or foot by the pinky or small toe) and progressive myopia. This condition was originally described in 9 persons in 4 generations of a family in Hungary in 1986. Family history suggests autosomal dominant inheritance.[1][2][3]
Last updated: 9/26/2013

References

  1. Polydactyly, Postaxial, with Progressive Myopia. Online Mendelian Inheritance in Man (OMIM). 1995; http://omim.org/entry/174310. Accessed 9/26/2013.
  2. Proust-Lemoine E. Polydactyly-myopia syndrome. Orphanet. October 2004; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=2917. Accessed 9/26/2013.
  3. Czeizel, A., Brooser, G. A postaxial polydactyly and progressive myopia syndrome of autosomal dominant origin. Clin. Genet. 1986; http://www.ncbi.nlm.nih.gov/pubmed/3802559. Accessed 9/26/2013.
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In Depth Information

  • The 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. 
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Polydactyly myopia syndrome. Click on the link to view a sample search on this topic.
Other Names for this Disease
  • Czeizel Brooser syndrome
  • PMS
  • Postaxial Polydactyly with progressive myopia
  • Postaxial polydactyly-progressive myopia syndrome
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.