Other Names for this Disease
- Absence or underdevelopment of the 6th and 7th cranial nerves
- Congenital facial diplegia
- Congenital facial diplegia syndrome
- Congenital oculofacial paralysis
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neurological condition that primarily affects the muscles that control facial expression and eye movement. Signs and symptoms of the condition may include weakness or paralysis of the facial muscles; feeding, swallowing, and choking problems; excessive drooling; crossed eyes; lack of facial expression; eye sensitivity; high or cleft palate; hearing problems; dental abnormalities; bone abnormalities in the hands and feet; and/or speech difficulties. Affected children often experience delayed development of motor skills (such as crawling and walking), although most eventually acquire these skills. Moebius syndrome is caused by the absence or underdevelopment of the 6th and 7th cranial nerves, which control eye movement and facial expression. Other cranial nerves may also be affected. There is no cure for Moebius syndrome, but proper care and treatment give many individuals a normal life expectancy.Moebius syndrome is a rare
Last updated: 7/15/2013
- Moebius syndrome. Genetics Home Reference. July 2010; http://ghr.nlm.nih.gov/condition/moebius-syndrome. Accessed 3/11/2011.
- NINDS Moebius Syndrome Information Page. National Institute of Neurological Disorders and Stroke, National Institutes of Health. September 16, 2008; http://www.ninds.nih.gov/disorders/mobius/moebius.htm. Accessed 3/11/2011.
- Genetics Home Reference (GHR) contains information on Moebius syndrome. This website is maintained by the National Library of Medicine.
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- 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.
- 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 Moebius syndrome. Click on the link to view a sample search on this topic.