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Genetic and Rare Diseases Information Center (GARD)

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McLeod neuroacanthocytosis syndrome


Other Names for this Disease

  • McLeod syndrome
  • X-linked McLeod syndrome
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Overview

McLeod neuroacanthocytosis syndrome is primarily a neurological disorder that occurs almost exclusively in males. Only about 150 cases have been reported worldwide. This condition affects movement in many parts of the body. People with this condition also have abnormal star-shaped red blood cells (acanthocytosis). This condition is one of a group of disorders called neuroacanthocytoses that involve neurological problems and abnormal red blood cells. McLeod neuroacanthocytosis syndrome is inherited in an X-linked recessive fashion and is caused by mutations in the XK gene.[1]
Last updated: 7/15/2011

References

  1. McLeod neuroacanthocytosis syndrome. Genetics Home Reference. May 2008; http://ghr.nlm.nih.gov/condition/mcleod-neuroacanthocytosis-syndrome. Accessed 7/15/2011.
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Basic Information

In Depth Information

  • The Online Mendelian Inheritance in Man (OMIM) is an 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 McLeod neuroacanthocytosis syndrome. Click on the link to view a sample search on this topic.
Other Names for this Disease
  • McLeod syndrome
  • X-linked McLeod 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.