Mobius Syndrome mobius syndrome, a rare genetic disorder characterized by facial paralysis, is caused by the absence or underdevelopment of the 6th and 7th cranial nerves. http://healthlink.mcw.edu/article/921441372.html
Extractions: Subscribe now >> Mobius syndrome, a rare genetic disorder characterized by facial paralysis, is caused by the absence or underdevelopment of the 6th and 7th cranial nerves. These nerves control eye movements and facial expression. In newborns, the first symptom is an inability to suck. Excessive drooling and strabismus (crossed eyes) may occur. Other symptoms may include lack of facial expression; inability to smile; feeding, swallowing, and choking problems; eye sensitivity; motor delays; high or cleft palate; hearing problems; and speech difficulties. Deformities of the tongue, jaw, and limbs, such as club foot and missing or webbed fingers, may also occur. Most patients have low muscle tone, especially in the upper body. Mental retardation may also occur. As children get older, lack of facial expression and inability to smile become the dominant visible symptoms. Mobius syndrome may be accompanied by Pierre Robin syndrome, a disease in which there is an abnormally small jaw, downward displacement of the tongue, and a soft, cleft palate. It may also be accompanied by Poland's anomaly, a disease characterized by abnormal development of one side of the chest and limb deformities.
NINDS Forwarding Page Also known as congenital facial diplegia, an information sheet compiled by NINDS. http://www.ninds.nih.gov/health_and_medical/disorders/mobius.htm
Mobius Syndrome mobius syndrome, a rare genetic disorder characterized by facial paralysis, is caused by the absence or underdevelopment of the 6th and 7th cranial http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Extractions: There is no specific course of treatment for Mobius syndrome. Treatment is supportive and in accordance with symptoms. Infants may require feeding tubes or special bottles to maintain sufficient nutrition. Surgery may correct crossed eyes and improve limb and jaw deformities. Physical and speech therapy often improves motor skills and coordination, and leads to better control of speaking and eating abilities. Plastic reconstructive surgery may be beneficial in some individuals. Nerve and muscle transfers to the corners of the mouth have been performed to provide limited ability to smile. What is the prognosis?
Mobius Syndrome Information Page National Institute Of mobius syndrome (Congenital Facial Diplegia) information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Introduction: Mobius Syndrome - WrongDiagnosis.com Introduction to mobius syndrome as a medical condition including symptoms, diagnosis, misdiagnosis, treatment, prevention, and prognosis. http://www.wrongdiagnosis.com/m/mobius_syndrome/intro.htm
Extractions: Mobius syndrome: Mobius syndrome, a rare genetic disorder characterized by facial paralysis, is caused by the absence or underdevelopment of the 6th and 7th cranial nerves. These nerves control eye movements and facial expression. Researching symptoms of Mobius syndrome: Further information about the symptoms of Mobius syndrome is available including a list of symptoms of Mobius syndrome , or alternatively return to research other symptoms in the symptom center Treatments for Mobius syndrome: Various information is available about treatments available for Mobius syndrome , or research treatments for other diseases.
Biology Symptoms, diagnosis, and treatment of mobius syndrome. Information on research, community outreach and support. http://genetics.about.com/science/genetics/library/blmob.htm
MOEBIUS SYNDROME NEWS NEWSLETTER MOBIUS SYNDROME CRANIAL NERVE Growing Old With Moebius. NACD. Annilea, A New Book. Moebius Syndrome Book. Questions/Answers. Thank You's. Gentler Method Club Foot. Mother http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Extractions: There is no specific course of treatment for Mobius syndrome. Treatment is supportive and symptomatic. Infants may require feeding tubes or special bottles to maintain sufficient nutrition. Surgery may correct strabismus and improve limb and jaw deformities. Physical and speech therapy may improve motor skills and coordination, and help to better control speaking and eating abilities. Plastic reconstructive surgery may be beneficial in some individuals. Also, in a few cases, nerve and muscle transfers (microvascular muscle transplant) to the corners of the mouth have been performed to provide some ability to smile. What is the prognosis?
Reader's Digest - Rd.com A list of alternate names for mobius syndrome, along with a general discussion and resources. http://www.rd.com/common/nav/index.jhtml?articleId=8612437
Mobius Syndrome mobius syndrome. This article submitted by Shawn K. Centers, DO on 4/14/95. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Mobius Syndrome mobius syndrome. This article submitted by Shawn K. Centers, DO on 4/14/95. mobius syndrome is a conginital disorder involving (1)complete or partial VIIth http://neuro-www.mgh.harvard.edu/neurowebforum/ChildNeurologyArticles/MobiusSynd
MOBIUS SYNDROME mobius syndrome. mobius syndrome is a rare congenital disturbance consisting of varying involvement of facial and lateral gaze paresis. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Mobius Syndrome understand it, current thinking suggests that mobius syndrome a literature search of mobius syndrome that was published (? in Peds http://neuro-www.mgh.harvard.edu/neurowebforum/ChildNeurologyArticles/MobiusSynd
MOEBIUS SYNDROME SUPPORT NETWORK HOMEPAGE Bringing together information from and links to medical and lay support for those affected by Moebius syndrome. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
Mobius Syndrome mobius syndrome. Synonym(s) Congenital Facial Diplegia. What is mobius syndrome? mobius syndrome, a rare genetic disorder characterized by facial paralysis http://www.clevelandclinic.org/health/health-info/docs/1300/1307.asp?index=6064&
Show-documents.asp mobius syndrome Written Information. Care Treatment. , mobius syndrome New Search Health Extra Menu. http://www.clevelandclinic.org/healthextra/do-query.asp?TopicId=1329
Mutation Analysis In The Candidate Mobius Syndrome Genes PGT And F, Brunoni D, Schwarz IV, Larrandaburu M, Safattle H, Meloni VF, Koren G. Use of misoprostol during pregnancy and Mobius' syndrome in infants. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126
MOBIUS SYNDROME mobius syndrome is a rare congenital disturbance consisting of varying Clinical Manifestations mobius syndrome is characterized by unilateral or http://www.members.aol.com/scottolitsky/mobius.htm
Extractions: Mobius syndrome is a rare congenital disturbance consisting of varying involvement of facial and lateral gaze paresis. Mobius first suggested that congenital bilateral abducens-facial paralysis might be an independent pathologic entity, thus gaining eponymic distinction. Clinical Manifestations Mobius syndrome is characterized by unilateral or bilateral inability to abduct the eyes. Although horizontal movements are usually lacking, vertical movements and convergence are intact. Pupillary constriction, vision, and the retina are generally normal. Congenital esotropia is common in children with Mobius syndrome. In a retrospective study of 61 patients with this syndrome, 38 per cent had early-onset esotropia. The unilateral or bilateral complete or incomplete facial palsy is usually observed during the first few weeks of life because of difficulty with sucking and feeding, and incomplete closure of the eyelids during sleep. These patients typically have masklike faces with an inability to grin and wrinkle the forehead. Mobius syndrome is frequently associated with paresis of other muscles supplies by the cranial nerves. Often, there is partial atrophy of the tongue with inability to protrude the tongue beyond the lips. Paralysis of the soft palate and muscles of mastication may also occur. Various skeletal and muscle defects are common, including absence or hypoplasia of the pectoral muscles, syndactyly, club feet, and congenital limb amputations.