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         Congenital Facial Diplegia:     more detail

21. Leslie
of two cases. med8589 327 The spectrum of congenital facial diplegia(Moebius syndrome). med75-79 327 Moebius syndrome. med93-95
http://neuro-www.mgh.harvard.edu/neurowebforum/ChildNeurologyArticles/Leslie.htm
Leslie
This response submitted by Dr. Shawn K. Centers on 12/19/96. Author's Email: Dear Leslie:
Although previuosly it was thought that there was an agenesis ( failure to develop )of the control centers for the cranial nerves ( especially cranial nerve VI and VII) some of the recent research seems to call this into question. If there is complete agenesis this means that there is no possibility of the facial paralysis improving or worsening. One recent report describes muscle recruitment measured by EMG studies in two Moebius patients following treatment with simple physical therapy. In another report there is described improvement in facial paralysis using biofeedback techniques
(the patients were both children). The Miami Project in FL seems to be the center that is doing the most research with biofeedback training in muscle paralysis. There is also a research center in England who claims to have gotten improvement in muscle hypotonia and facial paralysis using a type of tactile kinesthetic stimulation using "brushing technique" wirth a number of Moebius patients (mostly children). As of yet their research is unpublished. There are likewise reports of a Moebius patient's paralysis worsening and thought to be caused by a superimposed Bell's Palsy. When I was younger I recieved treatment at the Michigan State University
We really have very little to offer them at this time in terms of treatment. With better information we may be able to offer some suggestions

22. Moebius Syndrome And Possible Causes
Ziter et al. (1977) observed congenital facial diplegia and flexionfinger contractures in 7 members of 3 generations of a family.
http://neuro-www.mgh.harvard.edu/forum/MoebiusSyndromeF/3.21.982.19AMMoebiussynd
Moebius syndrome and Possible Causes
This article submitted by on 3/21/98.
Email Address:
The following is from "OMIM" - ONLINE MENDELIAN INHERITANCE IN MAN. This may lay to rest persistent remors re: the singular cause of Moebius being Herpes.... These are from various Moebius-related texts found at: http://www3.ncbi.nlm.nih.gov/htbin-post/Omim/getmim
Harbord et al. (1989) described a child with Moebius syndrome associated with unilateral cerebellar hypoplasia. Journel et al. (1989) described Moebius syndrome in 2 brothers and a male first cousin who were sons of sisters, thus suggesting X-linked recessive inheritance. The 2 brothers also had hypoplasia of the thumbs and absence of the big toes. Kawai et al. (1990) described the fourth case of Moebius syndrome (which they referred to as Moebius sequence) associated with peripheral neuropathy and hypogonadotropic hypogonadism. Pulsatile administration of gonadotropin-releasing hormone for 3 months was effective therapy. Kumar (1990) provided a review, which was critiqued by Lipson et al. (1990). MacDermot et al. (1991) urged that the term Moebius syndrome be restricted to cases with congenital sixth and seventh nerve paralysis with skeletal defects; according to their analysis, the recurrence risk is low (about 2%) in these cases. In their review, no recurrence was noted in 31 cases with cranial nerve palsies associated with oral abnormalities and limb defects. The features in an index case that may indicate a higher risk of recurrence are the absence of skeletal defects, isolated facial palsy, deafness, ophthalmoplegia, and digital contractures. As an example of the latter category, MacDermot et al. (1991) described mother and son with fifth, sixth, seventh, and bulbar cranial nerve paralysis who had 2 similarly affected relatives: the mother's maternal aunt and her son.

23. WebMD -
Synonyms congenital facial diplegia Syndrome; Congenital Oculofacial Paralysis;Mobius Syndrome; Moebieus Sequence. Disorder Subdivisions None. General Discussion.
http://my.webmd.com/NR/internal.asp?GUID={E7A1B26A-1D20-4DA5-93CB-EB1CF75ACE09}

24. MEDLINEplus: Facial Injuries And Disorders
and Stroke); Mobius Syndrome (congenital facial diplegia) (NationalInstitute of Neurological Disorders and Stroke); Orbital Trauma
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  • 25. MEDLINEplus: Birth Defects
    Drug Information); Mobius Syndrome (congenital facial diplegia) (NationalInstitute of Neurological Disorders and Stroke); Pregnancy
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    26. NORD - National Organization For Rare Disorders, Inc.
    View Cart/Checkout. Copyright 1987, 1990, 1995, 1998, 1999, 2000 Synonymsof Moebius Syndrome congenital facial diplegia Syndrome;
    http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Moebius Syndr

    27. YOUNG ONSET NEUROLOGICAL DISEASE ASSOCIATION Br YONDA For Short
    Coffin Lowry Syndrome, Coma, including Persistent Vegetative State, Complex RegionalPain Syndrome, congenital facial diplegia, Congenital Vascular Cavernous
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    28. Mestrado
    Translate this page Summary. Moebius syndrome, also known as congenital facial diplegia, comprisesan heterogeeneous group of conditions, caused by vascular disruption.
    http://www.unb.br/fs/dd_cesm.htm
    CARLOS EDUARDO SPECK MARTINS
    Nome do Autor: Carlos Eduardo Speck Martins
    Data da defesa: 04/01/2000.
    Nome do orientador: Riccardo Pratesi
    Summary
    Moebius syndrome, also known as congenital facial diplegia, comprises an heterogeeneous group of conditions, caused by vascular disruption. Its origin is probably environmental in the vast majority of the cases. There are some works on families with a mendelian pattern of inheritance. Some factors have been implicated in the genesis of the disorder: drugs acting as inductors of uterine contratility, maternal hypotension, maternal trauma and hyperthermia.
    In the present work we analyze 105 patients with Moebius syndrome seen in the ambulatorys of pediatrics and genetics at the Sarah Network of Hospitals. We studied the association between Moebius and vaginal bleeding. We also analyzed the following parameters: maternal hyperthermia and trauma in the first trimester and polyhydramnius.
    Our data confirm the statistical significance between Moebius syndrome and vaginal bleeding. We were not able to establish a causal relationship. It was also confirmed the relationship between the disease and ingestion of misoprostol in the first trimester of pregnancy.

    29. MSN Health -
    Synonyms congenital facial diplegia Syndrome; Congenital Oculofacial Paralysis;Mobius Syndrome; Moebieus Sequence. Disorder Subdivisions None. General Discussion
    http://content.health.msn.com/NR/internal.asp?GUID={E7A1B26A-1D20-4DA5-93CB-EB1C

    30. NINDS - Neurological Disorder Information
    Pain 23 Coffin Lowry Syndrome 24 Coma, including Persistent Vegetative State 25Complex Regional Pain Syndrome 26 congenital facial diplegia 27 Congenital
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    31. Mobius Syndrome
    Mobius Syndrome. Synonym(s) congenital facial diplegia What is MobiusSyndrome? Mobius syndrome, a rare genetic disorder characterized
    http://www.clevelandclinic.org/health/health-info/docs/1300/1307.asp?index=6064

    32. C Website Results :: Linkspider UK
    Arthromyodysplasia@ (96); congenital facial diplegia@ (5); CongenitalHeart Disease@ (53); Congenital Nephroblastoma@ (5); Congenital
    http://www.linkspider.co.uk/Health/ConditionsandDiseases/C/
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    treatment options. Mobius Syndrome Also known as congenital facial diplegia,an information sheet compiled by NINDS. Moebius Syndrome
    http://www.look.com/searchroute/directorysearch.asp?p=522991

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    Pain Syndromes (9); Compulsive Gambling (61); Congenital Arthromyodysplasia(96); congenital facial diplegia (5); Congenital Heart Disease
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    35. Genetic Approaches To Ocular Motility Disorders
    The three most commonly used minimal criteria are 1) congenital facial diplegia2) congenital facial diplegia and unilateral or bilateral loss of abduction 3
    http://mediswww.meds.cwru.edu/dept/neurology/ocular/full020.html
    GENETIC APPROACHES TO OCULAR MOTILITY DISORDERS
    Elizabeth C. Engle, M.D.
    Department of Anatomy and Neurobiology
    Children's Hospital
    Boston, MA, USA
    GENETICS OF CONCOMITANT STRABISMUS
    GENETICS OF INCOMITANT STRABISMUS

    Incomitant strabismus occurs when the misalignment or the angle of deviation of the eyes varies with gaze direction. This results from mechanical dysfunction in the orbit or neuromuscular dysfunction at the level of the muscle, nerve, or brainstem. Restricted neuromuscular disorders in this group include Duane syndrome, CFEOM, strabismus fixus, Möbius syndrome, and isolated cranial nerve palsies. Of these, the neuropathology of Duane and CFEOM have been described and have interesting parallels to one another. In addition, CFEOM, strabismus fixus, and some rare forms of Duane syndrome show clear patterns of inheritance, making them accessible to molecular genetic studies.
    1. "CLASSIC" CFEOM
    CFEOM has been a major focus of our laboratory investigations. Individuals with CFEOM have ptosis, infraductive strabismus, and severely restricted eye movements. The ophthalmoplegia is virtually complete with the eyes fixed at 20 to 40 degrees below the horizontal. Residual eye movements are typically in the horizontal plane and are often notable for aberrant and jerky convergent or divergent movements on attempted vertical gaze as well as retraction of the globe into the orbit. Affected individuals lack binocular vision, and frequently have significant refractive errors and amblyopia. We have noted hypotonia and mild gross motor delay in young affected children, and mild facial weakness in all affected individuals.

    36. Member Sign In
    when combined with methotrexate, may not induce abortion when taken alone; however,it can cause such anomalies as congenital facial diplegia (Möbius' syndrome
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    37. Tables
    MelkerssonRosenthal syndrome, Congenitally fissured tongue, orofacial edema, facialpalsy 5, Möbius' syndrome, congenital facial diplegia, ophthalmoplegia 6,
    http://www.medscape.com/content/2002/00/43/11/431188/431188_tab.html
    Tables for: Man With Facial Weakness
    Table 1. Differential Diagnosis for Bell's Palsy
    Disease Symptoms Diagnostic tools Melkersson-Rosenthal syndrome Congenitally fissured tongue, orofacial edema, facial palsy
    Congenital facial diplegia, ophthalmoplegia
    Ascending motor weakness, usually beginning in legs and possibly leading to respiratory muscle paralysis Nerve conduction velocity; electromyography Facioscapulohumeral muscular dystrophy Progressive weakness in the face, neck, upper torso, and upper arms Serum creatine kinase; electromyography Myasthenia gravis Weakness and fatigue, particularly of the extraocular, pharyngeal, facial, cervical, and respiratory musculature Computed tomography; electrodiagnostic studies Sarcoidosis Shortness of breath, cough, skin and ocular lesions; weakness, fatigue, fever, malaise Imaging studies; bronchoscopy; lymph node biopsy

    38. AnsMe Directory - Health > Conditions And Diseases > C
    Compulsive Gambling. Congenital Arthromyodysplasia. congenital facial diplegia.Congenital Heart Disease. Congenital Nephroblastoma. Congenital Pain Insensitivity.
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    39. Browsing Health Conditions And Diseases C Category
    Cold Communication Disorders Complex Regional Pain Syndromes Compulsive GamblingCongenital Arthromyodysplasia congenital facial diplegia Congenital Heart
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    Bilateral Bell's phenomenon is found in myasthenia gravis, sarcoidosis, bilateralBell's palsies, congenital facial diplegia, some rare forms of muscular
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