Chiari malformation type 2
Other Names for this Disease
- Arnold Chiari malformation type II
- Arnold-Chiari malformation
- Chiari malformation type II
- Chiari type II malformation
Chiari malformation in which both the cerebellum and brain stem tissue extend into the foramen magnum (the hole at the skull base for passing of the spinal cord). This form is often accompanied by a type of spina bifida called myelomeningocele, and can also be accompanied by syringomyelia, hydrocephalus, or other abnormalities. Symptoms in infants may include stridor (wheezing sound); difficulty swallowing (dysphagia); feeding difficulties; hypotonia; and weak cry. Symptoms in children and/or adults may include headache; fatigue; loss of vision; tingling extremities; nausea; dysphagia; dizziness; muscle weakness; and ataxia. Adults and adolescents who previously had no symptoms may begin to have symptoms later in life. The exact cause of the condition is not known but it appears to be due to a developmental failure of the brain stem and upper spine. The term Arnold-Chiari malformation is technically specific to type II but may sometimes be used to describe other types of Chiari malformations.Chiari malformation type 2 (CM type II) is a type of
Last updated: 8/8/2011
- Chiari Malformation Fact Sheet. NINDS. June 7, 2011; http://www.ninds.nih.gov/disorders/chiari/detail_chiari.htm. Accessed 8/8/2011.
- Arnold-Chiari Malformation. NORD. April 19, 2008; http://www.rarediseases.org/rare-disease-information/rare-diseases/byID/85/viewAbstract. Accessed 8/8/2011.
- Cassandra L. Kniffin. CHIARI MALFORMATION TYPE II. OMIM. August 9, 2006; http://omim.org/entry/207950. Accessed 8/8/2011.
- 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.
- 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.
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- 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.
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