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         Encephalofacial Angiomatosis:     more detail

61. Webum > Health > Conditions And Diseases > E
Elephantiasis@; Emetophobia@; Emphysema@; Empty Sella Syndrome@; Encephalitis@;encephalofacial angiomatosis@; Encephalomyelitis@; Enchondromatosis@.
http://www.en.webum.org/Health/Conditions_and_Diseases/E/
Webum Health Conditions and Diseases
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  • 62. Turn Of The Century - British Association Of Dermatologists
    Rare diseases and syndromes which are rightly associated with his name include Sturge-Kalischer-Weber (encephalofacial angiomatosis) Weber-Christian
    http://www.bad.org.uk/general/history/turn/
    Skin Facts News The Sarkany Interviews History of British Dermatology ... Index of Names
    Some Remarkable Clinicians
    On the whole little interest was taken in promoting dermatological knowledge at this time, nevertheless a few outstanding individuals were to make lasting impressions. In Manchester, Louis Savatard, Brooke's pupil, was meticulously analysing all the various cutaneous malignancies. Louis Savatard (1874-1942) was a pioneer of radiotherapy but it must have been Brooke's interest in pathology that set him on his way; he was to become an acknowledged expert, spending endless hours at his microscope. From 1920 to 1940 he published many papers on superficial and pre-malignant skin changes and his interest in "mulespinner's cancer", led to his appointment to the special Home Office Committee. He virtually founded both the North of England and the Manchester Dermatological Societies and was President of the BAD in 1940. Savatard worked in isolation, but he made Manchester aware of the subject at what was surely a barren period. In London one or two others were now to make a name for themselves and for dermatology.

    63. AnsMe Directory - Health > Conditions And Diseases > E
    Emetophobia. Emphysema. Empty Sella Syndrome. Encephalitis. encephalofacial angiomatosis.Encephalomyelitis. Enchondromatosis. Encopresis. EndStage Renal Disease.
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    64. Abducted Children
    Encephalitis. Encephalitis Society, Tel 01653 699 599. encephalofacial angiomatosis.contact Sturge Weber Foundation, Tel 01392 464 675. Encephalomyelitis Myalgia.
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    65. D - E
    ENCEPHALITIS, RESMUSSEN. See Rasmussen Syndrome. encephalofacial angiomatosis.ENCEPHALOTRIGEMINAL ANGIOMATOSIS. See SturgeWeber Syndrome. ENCEPHALOMYELOPATHY.
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    DANDY-WALKER SYNDROME
    See also: Hydrocephalus Dandy Walker Home Page http://www.geocities.com/Heartland/Hills/3919/dws.html NINDS Dandy Walker Syndrome Information Page http://www.ninds.nih.gov/health_and_medical/disorders/dandywalker.htm
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    See also: Autoimmune Disorders; Kidney Disorders American Diabetes Association http://www.diabetes.org

    66. Health Conditions And Diseases E
    9 Elephantiasis@ 8 Emetophobia@ 9 Emphysema@ 92 Empty Sella Syndrome@ 5Encephalitis@ 7 encephalofacial angiomatosis@ 4 Encephalomyelitis@ 2
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    67. HNet - Directory: Health Conditions And Diseases E
    9 Elephantiasis@ 8 Emetophobia@ 9 Emphysema@ 91 Empty Sella Syndrome@ 5Encephalitis@ 7 encephalofacial angiomatosis@ 4 Encephalomyelitis@ 2
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    68. Sturge-Weber Encephalotrigeminal (encephalofacial) Angiomatosis
    SturgeWeber encephalotrigeminal (encephalofacial) angiomatosis. Copyright © 2002 SimulConsult®Inc. - () Sturge-Weber encephalotrigeminal (encephalofacial) angiomatosis. This finding is discussed
    http://www.simulconsult.com/resources/c0038505.html
    Sturge-Weber encephalotrigeminal (encephalofacial) angiomatosis
    This finding is discussed in an NIH Information Sheet . Support group: Sturge-Weber Foundation
    SimulConsult
    Inc.

    69. Malattie Rare E Genetiche Lettera "W"
    angioma/ectoneurodermal hamartoma/encephalocraniofacial angiomatosis/encephalofacialangiomatosis/encephalofacial neuroangiomatosis/encephalotrigeminal
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    ... Waardenburg Sindrome di (denominazione generica) [Distopia epicantale-albinismo-sordità percettiva /Sindrome di Klein-Waardenburg/Distopia canthia medialis lateroversa/Sindrome ptosi-epicanto]/ Waardenburg tipo 1 Sindrome di Waardenburg tipo 2 Sindrome di Waardenburg tipo 3 Sindrome di Waardenburg tipo Pierpont ... Waardenburg, Síndrome de

    70. Penn State Faculty Research Expertise Database (FRED)
    Hemangiomatosis Syndrome, encephalofacial. Hemangiomatosis Syndromes, encephalofacial,Meningo Oculo Facial angiomatosis. MeningoOculo-Facial
    http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D013341

    71. PharmGKB: Sturge-Weber Syndrome
    Syndromes; Hemangiomatosis Syndrome, encephalofacial; Hemangiomatosis Syndromes,encephalofacial; Meningo Oculo Facial angiomatosis; MeningoOculo-Facial
    http://www.pharmgkb.org/do/serve?objId=PA445756&objCls=Disease

    72. Seizures And Skin Lesions
    SturgeWeber syndrome, also known as encephalofacial/encephalotrigeminal angiomatosis,is characterized by a facial port wine nevus and leptomeningeal
    http://www.medscape.com/viewarticle/438132_2

    73. Sturge-Weber Syndrome
    The Official Parent s Sourcebook on STURGEWEBER SYNDROME (Dimitri Disease; Encephalofacialangiomatosis; Encephalotrigeminal angiomatosis; Leptomeningeal
    http://www.icongrouponline.com/health/Sturge_Weber.html
    ICON Health Publications
    Official Health Sourcebooks The Official Parent's Sourcebook
    on
    STURGE-WEBER SYNDROME

    (Dimitri Disease; Encephalofacial Angiomatosis; Encephalotrigeminal angiomatosis; Leptomeningeal Angiomatosis; Meningeal Capillary Angiomatosis; Sturge-Kalischer-Weber Syndrome; Sturge-Weber Phakomatosis; Sturge-Weber-Dimitri syndrome) Revised and Updated for the Internet Age P A P E R B A C K Paperback Book Paperback Book Order by phone: 800-843-2665 (within USA) 1-201-272-3651 (from outside USA) Paperback Book Shipped in 3 to 5 business days
    E B O O K Electronic File * E-Book version sent via e-mail in 2 business days Electronic File *E-Book version sent via e-mail in 2 business days Pages Price $28.95(USD) ISBN Published Synopsis A comprehensive manual for anyone interested in self-directed research on Sturge Weber. Fully referenced with ample Internet listings and glossary. Related Conditions/Synonyms Dimitri Disease; Encephalofacial Angiomatosis; Encephalotrigeminal angiomatosis; Leptomeningeal Angiomatosis; Meningeal Capillary Angiomatosis; Sturge-Kalischer-Weber Syndrome; Sturge-Weber Phakomatosis; Sturge-Weber-Dimitri syndrome Description Table of Contents Introduction Overview Organization Scope Moving Forward PART I: THE ESSENTIALS Chapter 1. The Essentials on Sturge-Weber Syndrome: Guidelines

    74. ICON Health Publications -- Index
    Emphysema. Encephalitis lethargica. Encephalitis Periaxialis Diffusa. Encephalofacialangiomatosis. Encephalotrigeminal angiomatosis. End stage renal disease.
    http://www.icongrouponline.com/browse/Health/healthE.html
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    75. Glossary
    encephalofacial Refering to the face and the brain, as in encephalofacialAngiomatosis encephalopathy - Any degenerative brain disease.
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    Glossary A B C D ... Z abdominal - Pertaining to the abdomen usually the stomach and gastro-intestinal system abscess - An encapsulated area of infection abscesses - An encapsulated area of infection acromegaly - Excessive secretion of pituitary growth hormone in adults; it causes an abnormal enlargement of the extremities of the skeleton. ACTH - Adrenocorticotropic hormone, which is secreted by the anterior pituitary gland and has a stimulating effect on the adrenal cortex. Acute - Having a sudden onset. acutely - Having a sudden onset. adenoma - A benign epithelial tumor. adiposity - Obesity. AIDS - An immune deficiency illness caused by a virus. akinesia - Absense or poverty of movement.

    76. Sturge-Weber Syndrome
    BACKGROUND AND CLINICAL INFORMATION Head. Also known as encephalofacialangiomatosis or encephalotrigerminal angiomatosis. Characteristics
    http://moon.ouhsc.edu/kfung/JTY1/NeuroHelp/ZNG0IE06.htm
    Sturge-Weber Syndrome NeuroLearn NeuroHelp Malformations Background ... Gross Pathology BACKGROUND AND CLINICAL INFORMATION Head Also known as encephalofacial angiomatosis or encephalotrigerminal angiomatosis. Characteristics: congenital angiomatosis which involves the skin of the face and cervical area, mucous membranes, meninges, and choroid of the retina. Usually unilateral.The skin lesions ("nevus flammeus" or “port wine stain") usually involves the territories of the sensory branches of the5th nerve, especially the ophthalmic branch. The gross and microscopic pathology depends on the age of the individuals. Genetics: Sporadiac. No known hereditary factor but familial cases have been reported. Clinical: manifestations of cortical damage include convulsions, mental defect, and hemiparesis or hemianopia on the side contra- lateral to the lesion. Symptoms usually onset within the first year of life. Angioma in the choroid may lead to buphthalmos (in 70% of the cases) in infancy or to glaucoma in childhood. Treatment: surgical resection should be considered within the first 6 months of life if the patient has intractable seizure.

    77. HONselect - Sturge-Weber Syndrome
    Weber Syndrome, Neuroretinoangiomatosis - Phakomatosis, Sturge-Weber - AngiomatosisOculoorbital-Thalamic Syndrome - encephalofacial Hemangiomatosis Syndrome
    http://www.hon.ch/HONselect/RareDiseases/C04.557.645.375.850.html
    List of rare diseases: English Deutsch
    Language:
    MeSH term:
    Accepted terms:
    English: Sturge-Weber Syndrome - Neuroretinoangiomatosis
    - Phakomatosis, Sturge-Weber
    - Angiomatosis Oculoorbital-Thalamic Syndrome
    - Encephalofacial Hemangiomatosis Syndrome
    - Meningo-Oculo-Facial Angiomatosis
    - Meningofacial Angiomatosis-Cerebral Calcification Syndrome
    Français: STURGE-WEBER-KRABBE, MALADIE - ANGIOMATOSE ENCEPHALOTRIGEMINEE - ANGIOMATOSE NEUROCUTANEE - MALADIE KRABBE - MALADIE STURGE-WEBER-KRABBE - MALADIE WEBER - WEBER, MALADIE Deutsch: Sturge-Weber-Syndrom - Neuroretinoangiomatose - Phakomatose, Sturge-Weber - Hamartome, ektoneurodermale - Neuroektodermaldysplasie, kongenitale - Neurokutanes Syndrom - Weber-Dimitri-Syndrom Español: SINDROME DE STURGE-WEBER - NEURORRETINOANGIOMATOSIS - FACOMATOSIS DE STURGE-WEBER Português: SINDROME DE STURGE-WEBER - NEURORRETINOANGIOMATOSE - FACOMATOSE DE STURGE-WEBER HONselect ressources Definition: Yes Articles: Yes Images: No News: No Conferences: No Clinical trials: Yes Web sites: English Yes Français Yes Deutsch Yes Español No Português No Home About us Site map Feedback ... HONewsletter http://www.hon.ch/HONselect/RareDiseases/C04.557.645.375.850.html

    78. PORT-WINE STAINS AND STURGE-WEBER SYNDROME
    to on the face peripherally 7 . What is Sturge Weber Syndrome (EncephalofacialAngiomatosis)? SturgeWeber syndrome (SWS) is a non
    http://www.med.nus.edu.sg/paed/medical_education/postgraduate/neurology/potwine_
    PORT-WINE STAINS AND STURGE-WEBER SYNDROME Dr Ong Hian Tat
    Consultant, The Children's Medical Institute, National University Hospital W hat are Port Wine Stains?
    Cutaneous port wine stains (PWS) are present from birth and the colour changes with age as the infant grows. In the newborn, the PWS are often flat and pale pink in colour, but darkens with age to a deep red or dark purple colour (as in port-wine) as well as thicken and become more nodular. They were in the past erroneously referred to as capillary hemangiomas, but are in fact venous ectasias. They appear sporadically in 3 per thousand births with no sex predilection. Although often depicted to involve the first division of the trigeminal nerve on the forehead, it could also extend and be present in other parts of the body e.g. trunk and the limbs. Options of Treatment for Port Wine Stains Facial PWS are unsightly resulting in psychological problems such as low self-esteem, lack of self-confidence, and difficulties in social interaction. Thus, options for treatment need be considered despite the possibility of incomplete response or resolution. For older children and adults with PWS, one of the obvious methods is covering up using camouflage make-up. Some people may achieve the desired effects through experimenting with over-the-counter cosmetics. Advances in technology in the past two decades have made laser the standard of care for the management of PWS despite unanswered questions on the treatment results and long-term benefits

    79. E From Linkspider UK Health Directory
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    80. E Listing Part 1
    Helps teach children about their feelings an feelings of others. ENCEPHALOFACIALANGIOMATOSIS. (See STURGEWEBER SYNDROME). ENCEPHALOMYELOPATHY.
    http://www.childhealthinfo.com/eindexlist1.htm
    E EAR INFECTIONS, ETC. (See also HEARING AND SPEECH) Ear Infections in Your Child, by Kenneth Grundfast, M.D. 1987, from the National Children Hospital in Washington, DC Hearing Helpline, (800) EAR-WELL. Free brochures on the diagnosis, prevention and treatment of hearing loss in infants and children. Koko Bear's Big Earache, Preparing your child for ear surgery, by Vicky Lansky. Bantam American Academy of Otolaryngology, Head and Neck Surgery (AAOHNS), One Prince Street Alexandria, VA 22314 Nonprofit organization advances the science and art of medicine related to otolaryngology. Publications include: Dizziness and Motion Sickness Travel Otitis Media Advisory Council, c/o Otitis Media News Bureau P.O. Box 3376, Grand Central Station New York, NY 10163-3376 Supplies written information about ear infections, how to treat them, etc. Otitis Media: A Children's Story...for Parents, A 23-page book that explains about ear infections is published by: Lederle Laboratories, Public and Government Affairs, One Cynamid Plaza, Wayne, NJ 07470

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