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Sturge-weber Syndrome:     more detail

The Official Parent's Sourcebook on Sturge-Weber Syndrome: A Revised and Updated Directory for the Internet Age by Icon Health Publications, 2002-09-17 Sturge-Weber Syndrome: The Resource Guide for a Reason, a Season, and a Lifetime Sturge-Weber Syndrome Sturge-Weber Syndrome Sturge-Weber syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Deepti, MS Babu, 2005 Sturge-Weber syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Deepti, MS Babu, 2005 The Sturge-Weber syndrome by George Lionel Alexander, 1960 Sturge-Weber syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Christine Kelly, 2006 Sturge-Weber Syndrome by George Lionel Alexander, R.M. Norman, 1960-12 A fourth type of phakomatosis, Sturge-Weber syndrome, (Verhandelingen der Koninklijke Akademie van Wetenschappen te Amsterdam, Afdeeling Natuurkunde, 2. sect) by Bernard Brouwer, 1937 Neurocutaneous Disorders: Phakomatoses & Hamartoneoplastic Syndromes Brain involvement in Sturge-Weber.(SPECIAL NEEDS: REALIZING POTENTIAL): An article from: Pediatric News by Anne Comi, 2009-02-01 Skin syndromes may spring from one disease: Klippel-Trenaunay and Sturge-Weber.(Clinical Rounds): An article from: Skin & Allergy News by Jeff Evans, 2003-09-01

lists with details

21. Epilepsy Action: Sturge-Weber Syndrome
    234343). © Epilepsy Action 2004. sturgeweber syndrome. sturge-weber syndrome is usually a spasmodic occurrence - in other words it does not run in families.  
    http://www.epilepsy.org.uk/info/sturge.html
    
    Extractions: HOMEPAGE EMAIL NEWSLETTER EPILEPSY INFORMATION MEMBERSHIP AND SERVICES ... APPLE UK STORE Epilepsy Action is the working name of British Epilepsy Association and is a Registered Charity (Registered in England No. 234343) Sturge-Weber Syndrome The Sturge-Weber Syndrome (SWS) is a rare disease in which the presence of a birth mark (port wine stain), usually on one side of the face, is associated with an abnormality of the brain caused by abnormal blood vessels on the surface of the brain. This abnormality usually results in seizures or other problems. Sturge-Weber Syndrome is usually a spasmodic occurrence - in other words it does not run in families. Very rarely one or more family members may be affected. Symptoms The first abnormality noted in Sturge-Weber Syndrome is the birth mark which is present at birth. This is flat and deep red. It is due to abnormalities of the very small blood vessels in the skin. The most common site for the birth mark is the forehead on one side of the face, often coming down on to the cheek, nose or upper lip. Sometimes both sides of the face are involved and on occasions similar birth marks are present on other parts of the body. Seizures develop in nearly all patients with Sturge-Weber Syndrome. They may start at birth or later in the first year of life. They are usually partial motor seizures involving jerks of one side of the body only. The seizures may become generalised and evolve into other types such as drop attacks, myoclonic or infantile spasms. The seizures are often very frequent and prolonged seizures may occur.

22. MedlinePlus Medical Encyclopedia: Sturge-Weber Syndrome
    sturgeweber syndrome. Encephalotrigeminal angiomatosis Definition Return to top. sturge-weber syndrome is a rare disorder present at birth.  
    http://www.nlm.nih.gov/medlineplus/ency/article/001426.htm
    
    Extractions: @import url(http://www.nlm.nih.gov/medlineplus/images/advanced.css); Skip navigation Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Contents of this page: Sturge-Weber syndrome - legs Sturge-Weber syndrome - soles of feet Circulatory system Alternative names Return to top Encephalotrigeminal angiomatosis Definition Return to top Sturge-Weber syndrome is a rare disorder present at birth. It is characterized by a birthmark, usually on the face, known as a port wine stain (from too many blood vessels just beneath the skin) and neurologic problems. Causes, incidence, and risk factors Return to top The cause of Sturge-Weber is unknown. There is no known hereditary component. Symptoms Return to top Signs and tests Return to top X-rays, MRI, or CT scans are useful to look for associated problems. Treatment Return to top Treatment is based on the patient's signs and symptoms:

23. Sturge-Weber Syndrome
    sturgeweber syndrome. This response submitted by Bodo Kirtz on 4/12/96. Author s Email We have a son born in 1991 with Struge-Weber Syndrom.  
    http://neuro-www.mgh.harvard.edu/neurowebforum/ChildNeurologyArticles/SturgeWebe

24. Sturge-Weber Syndrome - Information / Diagnosis / Treatment / Prevention
    home genetic disorders sturgeweber syndrome sturge-weber syndrome. Information • Diagnosis • Treatment • Prevention. External  
    http://www.healthcyclopedia.com/genetic-disorders/sturge-weber-syndrome.html

25. AllRefer Health - Sturge-Weber Syndrome (Encephalotrigeminal Angiomatosis)
    sturgeweber syndrome. Alternate Names Encephalotrigeminal Angiomatosis. Definition. sturge-weber syndrome is a rare disorder present at birth.  
    http://health.allrefer.com/health/sturge-weber-syndrome-info.html
    
    Extractions: AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia

26. AllRefer Health - Sturge-Weber Syndrome Pictures & Images (Encephalotrigeminal A
    You are here AllRefer.com Health Diseases Conditions sturgeweber syndrome Pictures Images. sturge-weber syndrome.  
    http://health.allrefer.com/health/sturge-weber-syndrome-pictures-images.html
    
    Extractions: AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Sturge-Weber Syndrome - Legs Sturge-Weber syndrome is a disease that affects the skin and nervous system (neurocutaneous) and is associated with Port Wine Stain, red vascular markings on the face and other parts of the body (shown here on the legs). This is an unusual case, due to the large size of the lesion (extensive involvement). Occasionally seizures or learning disorders are also associated with Sturge-Weber syndrome. Sturge-Weber Syndrome - Soles of Feet This picture shows the soles of two feet involved with port wine stain. Port wine stains in the area of the ophthalmic branch of the trigeminal nerve, with ipsilateral vascular anomalies constitute the Sturge-Weber syndrome. Glaucoma, retinal detachment, calcification of the outer layers of the cerebral cortex, and seizures may also be seen.

27. Norsk Forening For Sturge-Weber Syndrom
    Norsk Forening for SturgeWeber syndrom. Norwegian Foundation for sturge-weber syndrome. (NFSW). Vi har lagt opp sidene våre med såkalte vinduer (frames).  
    http://home.c2i.net/knut.sletten/NFSW.htm

28. Sturge-Weber Syndrome
    sturgeweber syndrome, Book, Home Page.  
    http://www.fpnotebook.com/DER160.htm
    
    Extractions: Home About Links Index ... Editor's Choice document.write(code); Advertisement Dermatology Pediatrics Acne ... Ophthalmology Sturge-Weber Syndrome Fungus Candida Diaper Dermatitis Hematology and Oncology Nevus Sebaceus of Jadassohn ... Miliaria Assorted Pages Aplasia Cutis Congenita Klippel-Trenaunay-Weber Syndrome Mongolian Spot Smooth Muscle Hamartoma ... Subcutaneous Fat Necrosis Sturge-Weber Syndrome Book Home Page Cardiovascular Medicine Dentistry Dermatology Emergency Medicine Endocrinology Gastroenterology General Medicine Geriatric Medicine Gynecology Hematology and Oncology HIV Infectious Disease Jokes Laboratory Neonatology Nephrology Neurology Obstetrics Ophthalmology Orthopedics Otolaryngology Pediatrics Pharmacology Prevention Psychiatry Pulmonology Radiology Rheumatology Sports Medicine Surgery Urology Chapter Dermatology Index Acne Bacteria Blister Cardiovascular Medicine Dermatitis Dry Environmental Injury Examination Ophthalmology Fungus Hair Hematology and Oncology Hyperplasia Infectious Disease Laboratory General Nails Parasite Pediatrics Pharmacology Pigment Prevention Procedure Psychiatry Rheumatology Sebaceous Sports Medicine Sweat Symptom Evaluation Wart Page Pediatrics Index Acne Milia Acne Neonatorum Acne Pustular Melanosis Aplasia Cutis Congenita Bacteria Perianal Blister Erythema Toxicum Blister Suction CV Hemangioma CV Nevus Flammeus CV Nevus Simplex Dermatitis Diaper Endo Klippel-Trenaunay-Weber Eye Sturge Weber Fungus Diaper Hemeonc Nevus Sebaceus Hyperplasia Seborrhea Mongolian Spot Smooth Muscle Hamartoma SubQ Fat Necrosis

29. Sturge-Weber Syndrome, Cincinnati Children's Hospital Medical Center
    Conditions and Diagnoses. sturgeweber syndrome. What is sturge-weber syndrome? sturge-weber syndrome is a rare disease with no recognized hereditary component.  
    http://www.cincinnatichildrens.org/health/info/vascular/diagnose/sturge-weber-sy
    
    Extractions: Sturge-Weber syndrome is a rare disease with no recognized hereditary component. It consists of a red discoloration (portwine stain) involving the skin on the face. Usually the eyelids are also involved. The mucous membranes (lining of the mouth and nose) and the meninges (covering of the brain) can also be affected. The cause of Sturge-Weber is unknown and there are no known preventive measures. Return to Top What are the symptoms?

30. Virtual Children's Hospital: Paediapaedia: Sturge-Weber Syndrome
    Paediapaedia Neurological Diseases sturgeweber syndrome. http//www.vh.org/pediatric/provider/radiology/PAP/NeuroDiseases/SturgeWeber.html.  
    http://www.vh.org/pediatric/provider/radiology/PAP/NeuroDiseases/SturgeWeber.htm

31. Sturge-Weber Syndrome
    sturgeweber syndrome. What is sturge-weber syndrome? sturge-weber syndrome rarely affects other body organs. Is there any treatment?  
    http://www.clevelandclinic.org/health/health-info/docs/1300/1349.asp?index=6074&

32. HONselect - Sturge-Weber Syndrome
    English sturgeweber syndrome, - Neuroretinoangiomatosis - Phakomatosis, Sturge-Weber - Angiomatosis Oculoorbital-Thalamic Syndrome - Encephalofacial  
    http://www.hon.ch/HONselect/RareDiseases/C04.557.645.375.850.html

33. Sturge-Weber Syndrome
    sturgeweber syndrome. What is it? sturge-weber syndrome is also known as encephaiofacial angiomatosis. It is a rare, progressive  
    http://www.hmc.psu.edu/childrens/healthinfo/s/sturgeweber.htm

34. Sturge Weber Syndrome
    National Organization for Rare Disorders, Inc. Sturge Weber Syndrome. General Discussion. sturgeweber syndrome is composed of three major symptoms.  
    http://www.bchealthguide.org/kbase/nord/nord306.htm
    
    Extractions: It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Information on the following diseases can be found in the Related Disorders section of this report: Sturge-Weber Syndrome is composed of three major symptoms. Excessive blood vessel growths (leptomeningeal angiomas) are accompanied by accumulations of calcium inside the brain, and seizures. Facial birth marks (nevus flammeus) appear usually on one side of the face. Angiomas similar to those found in the brain can develop inside the eye, often with secondary glaucoma. Nevus Flammeus is a discoloration on the face which is the red color of port wine. In Sturge-Weber Syndrome this "port wine stain" is noted at birth and generally occurs on the same side of the head as the excessive blood vessel growths (leptomeningeal angiomatoses) in the brain which are accompanied by accumulations of calcium (intracranial calcifications). The port wine stain primarily occurs along the distribution of the trigeminal nerve in the face, although in some cases it does not appear at all. Approximately thirty seven percent of patients have portwine stains on both sides of the face. Involvement of the extremities or trunk, in addition to the face, occurs in up to thirty-six percent of patients. Although the discoloration usually affects only one side of the face, a slight extension over the midface occurs in approximately fifty percent of cases. The port wine stain tends to deepen in color with age, and nodular elevations may also develop.

35. Sturge-Weber Syndrome - Medical Dictionary Definitions Of Popular Medical Terms
    MedicineNet Home MedTerms medical dictionary AZ List sturgeweber syndrome. The main sign of sturge-weber syndrome is a port wine stain birthmark.  
    http://www.medterms.com/script/main/art.asp?articlekey=11273

36. Introduction: Sturge-Weber Syndrome - CureResearch.com
    Introduction sturgeweber syndrome. sturge-weber syndrome Rare birth defect with birthmark and brain effects. 1 Contents for sturge-weber syndrome  
    http://cureresearch.com/s/sturge_weber_syndrome/intro.htm

37. Disease Directory : Genetic Disorders : Sturge-Weber Syndrome
    Diseases Genetic Disorders sturgeweber syndrome. AllRefer Health - sturge-weber syndrome - Legs (Pictures, Images sturge-weber syndrome - Legs.  
    http://www.diseasedirectory.net/Genetic_Disorders/Sturge-Weber_Syndrome/default.
    
    Extractions: Ablepharon-Macrostomia Syndrome ... Genetic Disorders : Sturge-Weber Syndrome AllRefer Health - Sturge-Weber Syndrome - Legs (Pictures, Images ... Article : Choroidal Hemangioma with a bleed in Sturge-Weber ... - LETTER TO EDITOR Choroidal Hemangioma with a bleed in Sturge-Weber Syndrome: MRI. Sir,. The Sturge-Weber syndrome: comparison of MR and CT characteristics. eMedicine - Sturge-Weber Syndrome : Article by Ali Nawaz Khan ... - Sturge-Weber Syndrome. Last Updated: March 17, 2003, Caption: Picture 1. Sturge-Weber syndrome. Plain lateral skull radiograph demonstrates eMedicine - Sturge-Weber Syndrome : Article by James J Riviello ... - Sturge-Weber Syndrome. Last Updated: October 12, 2001, Table 1. Clinical Manifestations of Sturge-Weber Syndrome Risk of SWS with facial PWS, 8%. Epilepsy Action: Sturge-Weber Syndrome - Sturge-Weber Syndrome. The Sturge-Weber Syndrome is usually a spasmodic occurrence - in other words it does not run in families. Very Hopkins Sturge-Weber Syndrome Center - What is Sturge-Weber Syndrome? Dermatologic Features; Neurologic Features; Ophthalmologic Features Diagnosis of Sturge-Weber Syndrome;

38. Sturge-Weber Syndrome Information Diseases Database
    sturgeweber syndrome aka/or Sturge-Weber-Dimitri syndrome aka/or Neuroretinoangiomatosis Medical information linkssturge-weber syndrome specific sites.  
    http://www.diseasesdatabase.com/ddb12572.htm

39. Health Library -
    Sturge Weber Syndrome. Synonyms Disorder Subdivisions General Discussion Resources General Discussion. sturgeweber syndrome is composed of three major symptoms.  
    http://yalenewhavenhealth.org/library/healthguide/IllnessConditions/topic.asp?hw

40. Sturge Weber Syndrome - Quest Diagnostics Patient Health Library
    National Organization for Rare Disorders, Inc. Sturge Weber Syndrome. None. General Discussion. sturgeweber syndrome is composed of three major symptoms.  
    http://www.questdiagnostics.com/kbase/nord/nord306.htm
    
    Extractions: It is possible that the main title of the report is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Sturge-Weber Syndrome is composed of three major symptoms. Excessive blood vessel growths (leptomeningeal angiomas) are accompanied by accumulations of calcium inside the brain, and seizures. Facial birth marks (nevus flammeus) appear usually on one side of the face. Angiomas similar to those found in the brain can develop inside the eye, often with secondary glaucoma. The Arc (a national organization on mental retardation)

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