NINDS Mobius Syndrome Information Page mobius syndrome (Congenital Facial Diplegia) information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). http://www.ninds.nih.gov/health_and_medical/disorders/mobius.htm
Extractions: Mobius syndrome is a rare birth defect caused by the absence or underdevelopment of the 6th and 7th cranial nerves, which control eye movements and facial expression. The first symptom, present at birth, is an inability to suck. Other symptoms can include: feeding, swallowing, and choking problems; excessive drooling; crossed eyes; lack of facial expression; inability to smile; eye sensitivity; motor delays; high or cleft palate; hearing problems; and speech difficulties. Small or absent brain stem nuclei that control the cranial nerves, as well as decreased numbers of muscle fibers, have been reported. Deformities of the tongue, jaw, and limbs, such as clubfoot and missing or webbed fingers, may also occur. As children get older, lack of facial expression and inability to smile become the dominant visible symptoms. The prognosis for otherwise normal development is excellent in most cases.
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.
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 nerve palsy (2 http://neuro-www.mgh.harvard.edu/neurowebforum/ChildNeurologyArticles/MobiusSynd
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
About.com With Laura L. Jelliffe, Ph.D. Symptoms, diagnosis, and treatment of mobius syndrome. Information on research, community outreach and support. http://genetics.about.com/science/genetics/library/blmob.htm
IRSC - Rare Disorders, Mobius Syndrome The Internet Resources for Special Children (IRSC) Global disABILITY resource is dedicated to communicating information relating to the needs of children with disABILITIES on a global basis MCW http://www.irsc.org:8080/irsc/irscmain.nsf/sub?readform&cat=Rare Disorders&a
Readers Digest Health 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. mobius syndrome is a rare congenital disturbance consisting of varying Clinical Manifestations mobius syndrome is characterized by unilateral or bilateral inability http://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.
Mobius Syndrome mobius syndrome. As I understand it, current thinking suggests that mobius syndrome may result from a vascular field defect (ie. http://neuro-www.mgh.harvard.edu/neurowebforum/ChildNeurologyArticles/MobiusSynd
Mobius Syndrome Information Diseases Database mobius syndrome Moebius congenital oculofacial paralysis, Disease Database Information http://www.diseasesdatabase.com/sieve/item1.asp?glngUserChoice=31978
Mobius Syndrome - Information / Diagnosis / Treatment / Prevention home genetic disorders mobius syndrome mobius syndrome. About.com with Laura L. Jelliffe, Ph.D. Symptoms, diagnosis, and treatment of mobius syndrome. http://www.healthcyclopedia.com/genetic-disorders/mobius-syndrome.html
Extractions: Web Directory: About.com with Laura L. Jelliffe, Ph.D. Symptoms, diagnosis, and treatment of mobius syndrome. Information on research, community outreach and support. MCW Healthlink: Mobius Syndrome Details about this disease, including what it is, the causes, symptoms and treatment options. Mobius Syndrome Also known as congenital facial diplegia, an information sheet compiled by NINDS.
Mobius Syndrome mobius syndrome. Synonym(s) Congenital Facial Diplegia. What is mobius syndrome? mobius syndrome, a rare genetic disorder http://www.clevelandclinic.org/health/health-info/docs/1300/1307.asp?index=6064&
Show-documents.asp What s New. The Cleveland Clinic, mobius syndrome Written Information. Care Treatment. mobius syndrome. New Search1. The Cleveland http://www.clevelandclinic.org/health/search/do-query.asp?TopicId=1329
Search: - Info.co.uk Results for mobius syndrome from Info.co.uk metasearch. Find better search results from the Web, Yellow Pages and White Pages quickly and easily! http://dpxml.infospace.com/infocom.uk/results?otmpl=dog/webresults.htm&qkw=M
Mobius Syndrome - Condition, Disease, Or Disorder Article mobius syndrome Article relating to particular medical disease, condition, or disorder. mobius syndrome. What is mobius syndrome? http://www.stopgettingsick.com/Conditions/condition_template.cfm/2569/303/1
Extractions: Mobius Syndrome What is Mobius Syndrome? Is there any treatment? 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?
MOBIUS SYNDROME mobius syndrome. mobius syndrome is a rare congenital disturbance consisting of varying involvement of facial and lateral gaze paresis. 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.
Conditions And Diseases - Mobius Syndrome Top Links mobius syndrome Web Site Links. mobius syndrome Also known as congenital facial diplegia, an information sheet compiled by NINDS. http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Genetic_Diso
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