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McLeod neuroacanthocytosis syndrome
Other Names for this Disease
- McLeod syndrome
- X-linked McLeod syndrome
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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.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
Last updated: 7/15/2011
- McLeod neuroacanthocytosis syndrome. Genetics Home Reference. May 2008; http://ghr.nlm.nih.gov/condition/mcleod-neuroacanthocytosis-syndrome. Accessed 7/15/2011.
- Genetics Home Reference (GHR) contains information on McLeod neuroacanthocytosis syndrome. This website is maintained by the National Library of Medicine.
- The National Institute of Neurological Disorders and Stroke (NINDS) collects and disseminates research information related to neurological disorders. Click on the link to view information on this topic.
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.