Medical Dictionary: C - WrongDiagnosis.com acuminata; Confinement; Congenital; Congenital agammaglobulinemia; CongenitalCMV; congenital facial diplegia; Congenital immunodeficiency; http://www.wrongdiagnosis.com/lists/dictc.htm
Extractions: Did we miss something? Please tell your story or provide feedback or suggestions By using this site you agree to our and . Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our and Book Lists WrongDiagnosis.com
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
Extractions: 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)
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
C Conditions And Diseases Health English English Health Conditions and Diseases Musculoskeletal Disorders Congenital AnomaliesArthrogryposis ? congenital facial diplegia English Health Conditions http://www.interactiva.org/Dir/I/English/Health/Conditions_and_Diseases/C/
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
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
Extractions: Main Page See live article Alphabetical index 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 Canavan disease Carpal tunnel syndrome CTS Causalgia Central pain syndrome Central pontine myelinolysis Cephalic disorder Cerebral aneurysm Cerebral arteriosclerosis Cerebral atrophy Cerebral gigantism Cerebral palsy Charcot-Marie-Tooth disease Chiari malformation Chorea Chronic inflammatory demyelinating polyneuropathy (CIDP) Chronic pain Chronic regional pain syndrome Coffin Lowry syndrome Coma, including Persistent Vegetative State
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.
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
Extractions: To close this window, click on the "x" in the upper right hand corner of the window. URL of this page: http://www.nlm.nih.gov/medlineplus/facialinjuriesanddisorders.html General/Overviews Facial Injuries (American Association of Oral and Maxillofacial Surgeons) - Links to PDF File - http://www.aaoms.org/public/treatment_ed/patient_PDF/FacialInjuries.pdf Anatomy/Physiology Atlas of the Body: The Skull (American Medical Association) - Clinical Trials ClinicalTrials.gov: Craniofacial Abnormalities (National Institutes of Health) - Specific Conditions/Aspects Coffin Lowry Syndrome (National Institute of Neurological Disorders and Stroke) - Short Summary - http://www.ninds.nih.gov/health_and_medical/disorders/coffin_lowry.htm Craniofacial Syndrome Descriptions (Children's Craniofacial Association) - http://www.ccakids.com/hlpmesyndef.stm Craniosynostosis and Craniofacial Disorders (American Association of Neurological Surgeons) - http://www.neurosurgerytoday.org/what/patient_e/craniosynostosis.asp
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
Extractions: 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)
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
Extractions: 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.
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
Snippets Bilateral Bell s phenomenon is found in myasthenia gravis, sarcoidosis, bilateralBell s palsies, congenital facial diplegia, some rare forms of muscular http://www.studentbmj.com/back_issues/0801/education/275.html
Extractions: 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
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
Extractions: 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
Extractions: 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;
