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Hereditary neuralgic amyotrophy
Other Names for this Disease
- Amyotrophy, hereditary neuralgic, with predilection for brachial plexus
- Brachial plexus neuropathy, hereditary
- Hereditary brachial plexus neuropathy
- Neuritis with brachial predilection
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brachial plexus. Common signs and symptoms include episodes of severe pain and muscle wasting in one or both shoulders and arms. Attacks may be spontaneous or triggered (e.g., by exercise, childbirth, surgery, infection etc.). Secondary complications, such as decreased sensation, abnormal sensations (e.g., numbness and tingling), chronic pain, and impaired movement may develop overtime. Affected members in some families may share additional distinct physical and facial characteristics. Hereditary neuralgic amyotrophy can be caused by mutations in the SEPT9 gene. It is inherited in an autosomal dominant fashion.Hereditary neuralgic amyotrophy is a type of nervous system disease that affects the
Last updated: 5/18/2011
- Hereditary neuralgic amyotrophy. Genetic Home Reference. 2009; http://ghr.nlm.nih.gov/condition/hereditary-neuralgic-amyotrophy. Accessed 5/11/2011.
- Genetics Home Reference (GHR) contains information on Hereditary neuralgic amyotrophy. This website is maintained by the National Library of Medicine.
- The MerckManual online reference Web site provides information on plexus disorders in general. Click on MerckManual to view the information page.
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- The Online Mendelian Inheritance in Man (OMIM) database contains genetics resources that discuss Hereditary neuralgic amyotrophy. Click on the link to go to OMIM and review these resources.
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