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21. Medical Dictionary: C - WrongDiagnosis.com
acuminata; Confinement; Congenital; Congenital agammaglobulinemia; CongenitalCMV; congenital facial diplegia; Congenital immunodeficiency;
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  • 22. 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

    23. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/C
    Arthromyodysplasia@ (99); congenital facial diplegia@ (5); CongenitalHeart Disease@ (47); Congenital Nephroblastoma@ (4); Congenital
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    24. ScienceDaily -- Browse Topics: Health/Child_Health/Conditions_and_Diseases/Conge
    Congenital Disorders (0 links). congenital facial diplegia@ (5); CongenitalHeart Disease@ (47). Congenital Musculoskeletal Disorders@ (209);
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    Real Estate Lookup Front Page Today's Digest Week in Review Email Updates ... Conditions and Diseases Congenital Disorders (0 links) See Also: News about Congenital Disorders Silence Of The Genes: Researchers Provide Unique View Of Inherited Disorders And Cancer (June 1, 2004) full story Reduced Mitochondrial Function Important Mechanism In Aging (May 31, 2004) full story Figs May Inhibit Growth And Survival Of Harmful Microbes In Food (May 31, 2004) full story Researchers Discover That A Protein In Grape Skins Can Kill Cancer Cells (May 28, 2004)

    25. 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

    26. C Conditions And Diseases Health English
    English Health Conditions and Diseases Musculoskeletal Disorders Congenital AnomaliesArthrogryposis ? congenital facial diplegia English Health Conditions
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    27. MOEBIUS SYNDROME
    Name. MOEBIUS SYNDROME Synonyms. congenital facial diplegia (codes).mobius syndrome (codes). Definition. A syndrome of congenital facial
    http://malattierare.pediatria.unipd.it/pubblicaMR/mr_dx_ing.asp?mr=236

    28. List Of Neurological Disorders
    Persistent Vegetative State; congenital facial diplegia; Corticobasaldegeneration; Cranial arteritis; Craniosynostosis; CreutzfeldtJakob
    http://www.fact-index.com/l/li/list_of_neurological_disorders.html
    Main Page See live article Alphabetical index
    List of neurological disorders
    This is a list of major and frequently observed neurological disorders (e.g. Alzheimer's disease ), symptoms (e.g. back pain ), signs (e.g. aphasia ) and syndromes (e.g. Aicardi syndrome). A B C D ... Z
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    29. Volume 62 January - December 1939
    The congenital facial diplegia syndrome clinical features, pathology and aetiology.JL . Henderson. Pages 381 403. Part of the OUP Brain WWW service.
    http://www3.oup.co.uk/jnls/supplements/braini/hdb/Volume_62/Issue_04/620381.sgm.
    Volume 62: January - December 1939
    Issue 4: December 1939
    Abstract
  • The congenital facial diplegia syndrome: clinical features, pathology and aetiology
  • JL Henderson Pages: Part of the OUP Brain WWW service
    General Information
    Click here to register with OUP. This page is maintained by OUP admin Last updated 13 May 97 Part of the OUP Journals World Wide Web service Oxford University Press, 1997

    30. Facial Injuries And Disorders (Print Version)
    Mobius Syndrome (congenital facial diplegia) (National Institute of NeurologicalDisorders and Stroke) Short Summary - http//www.ninds.nih.gov
    http://www.nlm.nih.gov/medlineplus/print/facialinjuriesanddisorders.html
    To print this page, use the print option from your browser.
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    Facial Injuries and Disorders
    URL of this page: http://www.nlm.nih.gov/medlineplus/facialinjuriesanddisorders.html

    31. Medical Diagnosis W/High Probability Of Developmental Delay
    742.1. Microcephaly. 352.6. Mobius (Poland) Syndrome (congenital facial diplegia,Mobius II). 272.7. Mucolipidosis. 277.5. Mucopolysaccharidosis. 359.0.
    http://www.eci.state.tx.us/oed/MedicalDiagnosis.htm
    Medical Diagnoses with High Probability of Developmental Delay The following is a list of medical diagnoses (sorted alphabetically) that qualify children as eligible for services. The list may change over time. A program director may request that a medical diagnosis be added by contacting the Director of Program Services. The Director of Program Services will work with a panel of physicians to establish that the medical diagnosis is recognized in the International Classification of Diseases and that the diagnosis has a high probability of developmental delay. Diagnoses recently added are in bold type. ICD-9 Code Diagnosis Achondrogenesis I (Parenti-Fraccaro Syndrome) Achondrogenesis II (Langer-Saldino Syndrome) Achondroplasia Acrodysostosis (Acrodysplasia I) Adrenoleukodystrophy Agenesis of the Corpus Collosum Alper's Disease (Poliodystrophy) Amelia, Lower Limb Amelia, Unspecified as to Site Amelia, Upper Limb Amniotic Band (affecting fetus or newborn) Anencephaly Angelman's Syndrome Anoxic Insult to Brain Apert's Syndrome (Acrocephalosyndactyly I, ACS I)

    32. Clinician Reviews: At Risk In Utero
    when combined with methotrexate, may not induce abortion when taken alone; however,it can cause such anomalies as congenital facial diplegia (Mobius syndrome
    http://articles.findarticles.com/p/articles/mi_m0BUY/is_1_10/ai_62276766
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    Previously, the only options for a fetus with amniocentesis-identified anomalies were termination of pregnancy or anticipatory guidance. Now, an increasing number of fetal anomalies can be treated prenatally. However, performing amniocentesis appears to be riskier during the first trimester than the second, reported Cynthia J. Curry, MD, of the University of California in San Francisco. According to results of the Canadian Early and Mid-trimester Amniocentesis Trial, earlier amniocentesis was associated with an increased rate of fetal loss, cell culture failure, amniotic fluid leakage, fetal contractures, and clubfoot. Effects of procedures performed at 11 weeks through 12 weeks, 6 days of gestation were compared with those at 15 weeks through 16 weeks, 6 days. Dr. Curry described several current treatments for prenatally diagnosed disorders. Pregnant women found to be immunoglobulin M-positive for Parvovirus infection can undergo ultrasound monitoring for signs of ascites; affected fetuses can then receive in utero transfusion. Fetal urethral obstruction can also be treated in utero via catheter drainage of the bladder. Diaphragmatic hernia can be resolved by plugging the fetal trachea to promote lung growth.

    33. OMIM - 134100 FACIAL PALSY, CONGENITAL UNILATERAL OR BILATERAL
    Autopsy in 3 cases showed partial agenesis of the facial motor nucleus. Wittig etal. (1967) observed congenital facial diplegia in 3 generations of a family.
    http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?cmd=entry&id=134100

    34. Snippets
    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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    Snippets A 69 year old patient presented for arthroscopic knee surgery. Her husband, a doctor with severe Parkinson's disease, had been mistakenly resuscitated against his wishes and died three weeks later in the intensive care unit. After this event the patient had written a living will to ensure that no such confusion would occur in her case. A living will should be sufficient in making clear a patient's wishes, but in order to further clarify her instructions, she had also had the words "Do Not Resuscitate" tattooed on her left chest wall. The arthroscopy was completed without adverse event under regional anaesthesia. C McCartney assistant professor Glen McGuire assistant professor, department of anesthesia and pain management, Toronto Western Hospital, Toronto, Canada
    J Smith

    35. ADC -- Abstracts: Jardine Et Al. 71 (3): 221
    congenital facial diplegia and sensorineural deafness in three children suggestthat infantile FSHD is not a genetically separate disorder from FSHD.
    http://adc.bmjjournals.com/cgi/content/abstract/archdischild;71/3/221

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    De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1)
    PE Jardine, MC Koch, PW Lunt, J Maynard, KD Bathke, PS Harper and M Upadhyaya
    Institute of Child Health, Bristol. Facioscapulohumeral muscular dystrophy (FSHD) is an autosomal dominant condition with variable age of onset and severity. Identification of a de novo DNA fragment by probe p13E-11 (D4F104S1) established the diagnosis of new mutation FSHD in 27 of 31 sporadic cases. The clinical data for these certain new mutation cases were as follows: 13 boys, 14 girls; mean age of onset 6.8 years; significant leg weakness in 19/27 (70%) (8/27 (30%) used wheelchairs at a mean age of 17.7 years); high tone sensorineural deafness in 10/27; visual acuity and direct ophthalmoscopy were normal. Congenital

    36. ORPHANET® : Base De Données Sur Les Maladies Rares Et Les Médicaments Orpheli
    craniosynostosis maternal hyperthyroidism Congenital cystic eye multiple ocularand intracranial anomalies congenital facial diplegia Congenital fiber type
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    37. Any Search Info - Directory: Health Child Health Conditions And Diseases Congeni
    Category contains information about congenital facial diplegia, congenital heartdisease, congenital musculoskeletal disorders, congenital nephroblastoma
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    38. Health/Conditions And Diseases/C
    Disorders@ 400 Complex Regional Pain Syndromes@ 7 Compulsive Gambling@ 76 CongenitalArthromyodysplasia@ 98 congenital facial diplegia@ 5 Congenital
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    39. Congress Autism-Europe Barcelona96. Proceedings.
    Fetal alcohol syndrome, Hypomelanosis of Ito, Joubert syndrome, LujanFryns syndrome,Moebius syndrome (congenital facial diplegia), Neurofibromatosis, Rett
    http://www.autismo.com/scripts/articulo/smuestra.idc?n=26B

    40. Hum. Mol. Genet. -- Kremer Et Al. 5 (9): 1367
    3 Hendersen , JL ( 1939 ) The congenital facial diplegia syndrome. Brain 62, 381403. 8Hellstrom , B. ( 1949 ) congenital facial diplegia. Acta Paediatr.
    http://hmg.oupjournals.org/cgi/content/full/5/9/1367
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    Human Molecular Genetics Pages
    Introduction

    Results
    Discussion Materials And Methods ... References
    Hannie Kremer Lambertus P. Kuyt Bellinda van den Helm Margo van Reen Jack A. M. Leunissen Ben C. J. Hamel Cees Jansen Edwin C. M. Mariman Rune R. Frants
    and George W. Padberg Departments of Human Genetics and Neurology, University Hospital Nijmegen, PO Box 9101, 6500 HB Nijmegen The Netherlands Department of Human Genetics, Free University, Amsterdam The Netherlands Caos Camm Center, Nijmegen The Netherlands Hospital Gelderse Vallei, Bennekom The Netherlands and MGC-Department of Human Genetics, Leiden University, Leiden The Netherlands Received April 23, 1996;

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