21. Sturge-Weber Syndrome Information Page: National Institute Of Neurological Disor sturgeweber syndrome (encephalotrigeminal angiomatosis) information sheet compiledby the National Institute of Neurological Disorders and Stroke (NINDS). http://www.ninds.nih.gov/disorders/sturge_weber/sturge_weber.htm

Accessible version Science for the Brain The nation's leading supporter of biomedical research on disorders of the brain and nervous system More about Sturge-Weber Syndrome Studies with patients Research literature Press releases Search NINDS... (help) Contact Us My Privacy NINDS is part of the National Institutes of Health You are here: Home Disorders Sturge-Weber Syndrome NINDS Sturge-Weber Syndrome Information Page Synonym(s): Encephalotrigeminal Angiomatosis Get Web page suited for printing Email this to a friend or colleague Table of Contents (click to jump to sections) What is Sturge-Weber Syndrome? Is there any treatment? What is the prognosis? What research is being done? ... Organizations What is Sturge-Weber Syndrome? Is there any treatment? Treatment for Sturge-Weber syndrome is symptomatic. Laser treatment may be used to lighten or remove the birthmark. Anticonvulsant medications may be used to control seizures. Surgery may be performed on more serious cases of glaucoma. Physical therapy should be considered for infants and children with muscle weakness. Educational therapy is often prescribed for those with mental retardation or developmental delays. Doctors recommend yearly monitoring for glaucoma. What is the prognosis?

22. Sturge-Weber Syndrome (www.whonamedit.com) sturgeweber syndrome A congenital disorder involving the brain, skin and eyes. Also known as Dimitri's hemangiomatosis syndrome Jahnke's http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

23. Sturge-Weber Syndrome / Family Village Library Sturge Weber Foundation United Kingdom Sturge Weber Syndrome Support Groupof New Zealand Norwegian Foundation for sturge-weber syndrome (NFSW) http://www.familyvillage.wisc.edu/lib_stur.htm

Sturge-Weber Syndrome Related Disorders: Sturge-Weber-Dimitri Syndrome, Klippel Trenaunay Syndrome , Sturge-Weber Phakomatosis Who to Contact Where to Go to Chat with Others Learn More About It Web Sites ... Search AltaVista for "Sturge-Weber Syndrome" Who to Contact Sturge-Weber Foundation (SWF) PO Box 418 Mt. Freedom, New Jersey, USA 07970 Fax: (973) 895-4846 E-mail: SWF@sturge-weber.com Website: http://www.sturge-weber.com/ The Sturge-Weber Foundation is a clearinghouse for information concerning Sturge-Weber Syndrome, Klippel Trenaunay, and Port Wine Stain Birthmarks. The Foundation provides support for parents and individuals with all three syndromes, educates the general public, medical profession, and government agencies, and funds research. The Foundation has local support groups and a directory in the form of area representatives and international resource contacts. They will assist individuals who wish to start a local chapter in their area and will provide parent-to-parent matching after receiving a signed permission form. The Sturge-Weber Foundation publishes a quarterly newsletter

24. BBC - Health - Ask The Doctor - Birthmarks For example, in a few cases there's a condition known as sturgeweber syndrome, where there may be abnormalities of the brain and eyes with http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

25. Epilepsy Action: Sturge-Weber Syndrome Brain The sturgeweber syndrome (SWS) is a rare disease in which the sturge-weber syndrome is usually a spasmodic occurrence - in other words it does http://www.epilepsy.org.uk/info/sturge.html

HOMEPAGE EPILEPSY INFORMATION FREE EMAIL UPDATES OUR SERVICES ... RESEARCH NEWS SHOP AND DONATE EPILEPSY ACTION SHOP TESCO ONLINE GROCERIES AMAZON.CO.UK and more Epilepsy Action is a working name of British Epilepsy Association. British Epilepsy Association 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

26. Sturge-Weber Syndrome (www.whonamedit.com) sturgeweber syndrome A congenital disorder involving the brain, skin and eyes.Also known as Dimitri’s hemangiomatosis syndrome,Jahnke s syndrome http://www.whonamedit.com/synd.cfm/1764.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A recommendation: Hypography is an open community about science and all things related Sturge-Weber syndrome Also known as: Dimitri’s hemangiomatosis syndrome Jahnke's syndrome (variant without glaucoma) Kalischer's syndrome Krabbe's syndrome II Lawford's syndrome Lawford’s meningocutaneous syndrome Miller's syndrome Parkes Weber-Dimitri syndrome Schirmer's syndrome Sturge's syndrome Sturge-Kalischer-Weber syndrome Sturge-Parkes Weber-Dimitri syndrome Sturge-Weber-Krabbe syndrome Sturge-Weber-Thoma syndrome Weber's syndrome Weber-Dimitri syndrome Synonyms: Angioma capillare et venosum calcificans, angiomatosis encephalofacialis, cerebrocutaneous angiomatosis, congenital neuroectodermal dysplasia, cutaneocerebral angioma, cutaneodermal angioma, encephalocutaneous angiomatosis, encephalofacial angiomatosis, encephalofacial neuroangiomatosis, encephalotrigeminal syndrome, encephalotrigeminal angiomatosis, encephalotrigeminal vascular syndrome, facial-meningeal angiomas, fourth phacomatosis syndrome, meningeal capillary angiomatosis, meningofacial angiomatosis, meningo-oculofacial angiomatosis, neuroangiomatosis encephalofacialis, neurocutaneous syndrome, neuroectodermal hamartoma, neuro-oculocutaneous angiomatosis, neurooculocutaneous syndrome, naevoid amentia, trigemino-encephalo-angiomatosis, phacomatosis syndrome, vascular encephalotrigeminal syndrome.

27. STURGE-WEBER SYNDROME: Contact A Family - For Families With Disabled Children: I Contact a Family is a UK charity for families with disabled children. We offerinformation on specific conditions and rare disorders. http://www.cafamily.org.uk/Direct/s63.html

printer friendly STURGE-WEBER SYNDROME home how we can help medical information index of conditions ... how you can help Did you find this page helpful? yes no Sturge-Weber syndrome (SWS) is a congenital disorder involving the brain, skin and eyes. There is a facial birth mark (port wine stain), a layer of blood vessels over the covering of the brain (venous angioma of the leptomeninges) and there may be an angioma (collections of abnormal blood vessels) involving the inner lining of the eye (choroidal angioma). The angioma usually involves one side of the brain and varies in extent. More rarely it may involve both sides of the brain. The port wine stain involves the skin around the eye, forehead or scalp. In some cases it may involve other areas of the body in addition to the typical facial distribution. In approximately 13 per cent of cases of SWS the facial port wine stain may be absent. Other features may include epilepsy in 75-90 per cent of cases, learning disability , hemiparesis (weakness of one side of the body) which may be evident during infancy or may occur in relation to seizures or in association with migraine-like headache, glaucoma (raised pressure in the eye) and episodic migraine-like headache.

28. 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. The http://neuro-www.mgh.harvard.edu/neurowebforum/ChildNeurologyArticles/SturgeWebe

Sturge-Weber 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. The doctors doesn't make us hope for his life, because the said his brain would be defect by 1/3. Today our son is in the kindergarden. His development is nearly normal. He has a little problem with spastic at the right side, but we think that in time the problems will disappear. Please contact us if you have, or need information: KirtzComputer@T-online.de yours Bodo Kirtz Next Article Previous Article Return to Main Article Article complete. Click HERE to return to the Neurology Web-Forum Menu.

29. Sturge-Weber Syndrome Community The sturgeweber syndrome Community provides information, resources, and supportto those living with sturge-weber syndrome. http://swscommunity.org/

Home About Us Group Login Ask An Expert ... Read Hank Bartenbach's Journal. Hank is having surgery to reduce port wine stain growth, and TLC is filming his saga. WELCOME TO THE STURGE-WEBER SYNDROME COMMUNITY A worldwide community for individuals and families living with Sturge-Weber Syndrome This site is dedicated to the adults and children living with SWS, and their families and friends. Each case of SWS is unique to the individual. The needs of a patient can vary greatly, depending on the symptoms and their severity. We hope the information provided on this site will prove beneficial to those seeking help and answers about SWS. Please contact the SWSC if you need further help or information, or if you have any suggestions or comments. Conference Notes www.birthmark.org. Dr. Stuart Nelson will deliver the keynote address and other speakers include Dr. Milton Waner, Dr. Martin Mihm and Dr. Ann Comi. Dr. Waner will present on surgical needs, Dr. Mihm will present on new research and Dr. Comi will present on Sturge-Weber Syndrome. There will be two teams for the clinic. Dr. Waner will be the surgeon on Team A and Dr. Marcelo Hochman will be the surgeon on Team B. Dr. Delfanian, VBF's Ask the KT expert will also be presenting on KT Syndrome and our Ask the Eye Specialist, Dr. Fay will be attending the clinic and conference to answer questions regarding eye conditions and vascular birthmarks.

30. Index Of /HopkinsSWSCenter/ Clinical center dedicated to the treatment and study of SWS at Johns HopkinsHospital in Baltimore. Find disease information, diagnosing, and treatment as http://www.neuro.jhmi.edu/HopkinsSWSCenter/

Index of /HopkinsSWSCenter/ Name Last modified Size Description Parent Directory Library/ 20-Jan-04 17:17 0K Templates/ 20-Jan-04 17:13 0K 20-Jan-04 17:13 0K clinical/ 20-Jan-04 17:20 0K contact.htm 20-Jan-04 16:29 10K diagnosis.htm 20-Jan-04 16:29 8K evals/ 20-Jan-04 17:20 0K funding.htm 21-Jan-04 11:59 9K glossary.htm 20-Jan-04 16:29 8K help.htm 20-Jan-04 16:29 8K images/ 15-Jun-04 16:45 0K index.htm 20-Jan-04 16:29 7K links.htm 02-Nov-04 16:55 8K photos/ 15-Jun-04 16:46 0K pngs/ 20-Jan-04 17:15 0K services/ 20-Jan-04 17:14 0K services.htm 20-Jan-04 16:29 9K sitemap.htm 20-Jan-04 16:29 10K staff/ 15-Jun-04 16:47 0K staff.htm 15-Jun-04 04:20 9K sws.htm

31. Hopkins Sturge-Weber Syndrome Center An overview of the sturgeweber syndrome Center at Johns Hopkins. http://www.neuro.jhmi.edu/HopkinsSWSCenter/funding.htm

The Johns Hopkins - Kennedy Krieger Institute Sturge-Weber Syndrome Center is funded through the generous support of two foundations, The Sturge-Weber Foundation and Hunter's Dream for a Cure The Sturge-Weber Foundation's mission is to improve the quality of life for individuals with port wine stains, Sturge-Weber Syndrome and Klippel-Trenaunay Syndrome. The Foundation strives to meet this goal by providing worldwide education and support and by facilitating research that could ultimately lead to a cure. Hunter's Dream for a Cure helps raise money for children with Sturge-Weber Syndrome and other neurological diseases. The foundation strives to provide necessary funding to facilitate research that could ultimately lead to a cure, a grant program for affected children and their families and funding for special needs programs in Colorado. If you would like support the Johns Hopkins - Kennedy Krieger Institute Sturge-Weber Syndrome Center, please contact: Katie Coyle, CFRE

32. Sturge-Weber Syndrome Information Diseases Database sturgeweber syndrome,Sturge-Weber-Dimitri syndrome,Neuroretinoangiomatosis,Disease Database Information. http://www.diseasesdatabase.com/ddb12572.htm

Diseases Database Index Sponsors Contact ... Previous Page Sturge-Weber syndrome information Search 3 synonyms or equivalents were found. Sturge-Weber syndrome aka/or Sturge-Weber-Dimitri syndrome aka/or Neuroretinoangiomatosis may cause or feature (Follow link for list.) may be associated with (Follow link for list.) belong(s) to the category of (Follow link for list.) Sturge-Weber syndrome: Definition(s) via UMLS Code translations and terms via UMLS Sturge-Weber syndrome: specific web sites Send Sturge-Weber syndrome to medical search engines (JavaScript enabled browsers only.) If your browser has no JavaScript you can still use these: Search using Internet medical databases Search using Internet search engines (non-specialist) We subscribe to the HONcode principles of the Health On the Net Foundation Valid XHTML 1.0 Served 2005-09-09 20:10:10 View metadata Last major update 2005-09-03. The medical information here is presented for education, background reading and general interest. The Diseases Database is not a diagnostic or clinical decision-making tool. Please consult your own licensed physician regarding diagnosis and treatment of any medical condition!

33. ► Sturge-Weber Syndrome A medical encycopedia article on the topic sturge-weber syndrome. http://www.umm.edu/ency/article/001426.htm

var MenuLinkedBy='AllWebMenus [2]', awmBN='530'; awmAltUrl=''; Disease Nutrition Surgery Symptoms Injury ... Encyclopedia (English) Toggle English Spanish Sturge-Weber syndrome Overview Symptoms Treatment Prevention Definition: A rare and sporadically occurring disease without a recognized hereditary component. It consists of multiple vascular lesions (angiomas) involving the skin of the face, mucus membranes, and covering of the brain (meninges). Alternative Names: Encephalotrigeminal angiomatosis; Sturge-Weber-Dimitri syndrome Causes, incidence, and risk factors: The cause of Sturge-Weber is unknown. Because of its spotty appearance in the population, specific risk factors are not yet recognized. Sturge-Weber syndrome - legs Sturge-Weber syndrome - soles of feet Circulatory system Review Date: 12/3/2001 Reviewed By: David G. Brooks, M.D., Ph.D., Division of Medical Genetics, University of Pennsylvania Medical Center, Philadelphia, PA. Review provided by VeriMed Healthcare Network.

34. Sturge-Weber Syndrome - Legs - UMMC sturgeweber syndrome is a disease that affects the skin and nervoussystem (neurocutaneous) and is associated with Port Wine Stain, red vascular markings http://www.umm.edu/imagepages/2536.htm

var MenuLinkedBy='AllWebMenus [2]', awmBN='530'; awmAltUrl=''; Home Medical Reference Encyclopedia (English) Toggle English Spanish 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. Acquired Date: 1/1/1997 12:00:00 AM Acquired From: Mosby Publishing Company

35. Sturge-Weber Syndrome sturgeweber syndrome (Encephalotrigeminal Angiomatosis, Sturge-Weber Angiomatosis).A rare cevelopmental condition characterized by a vascular birthmark http://www.dental.mu.edu/oralpath/lesions/sturgeweber/sturgeweber.htm

Sturge-Weber Syndrome (Encephalotrigeminal Angiomatosis, Sturge-Weber Angiomatosis) A rare cevelopmental condition characterized by a vascular birthmark and neurological abnormalities. Clinical Features: first year of life epilepsy, hemiplegia (a weakness or stiffness affecting one side of the body, glaucoma and learning difficulties. port wine stain usually involving at least one upper eyelid and the forehead usually unilateral, but bilateral cases can occur Etiology: unknown Tissue of Origin: vascular and neurological tissue Main Pathologic Process: developmental Treatment: no cure treat symptoms laser for cosmetic reasons Prognosis: disease itself is not fatal developmental delay emotional and behavioral problems special education requirements employment problems Webmaster © 2001 - Marquette University School of Dentistry - P.O. Box 1881 - Milwaukee, WI 53201-1881

36. Sturge-Weber Syndrome Review what might cause a baby to have facial paralysis and a port wine stain. http://pediatrics.about.com/od/weeklyquestion/a/05_sturge_weber.htm

var zLb=1; zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a12' About Pediatrics Medical Advice Diseases and Conditions ... Birthmarks Sturge-Weber syndrome Pediatrics Essentials Baby Names Ideal Body Weight Calculator ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/7.htm','');w(xb+xb); FREE Newsletter Sign Up Now for the Pediatrics newsletter! See Online Courses Search Pediatrics Stay up to date! Compare Prices Email to a friend ... Print this page Pediatric Resources Pediatric Problem Solver Ages and Stages More Pediatric Resources Symptom Checker Medical Advice Pediatric Basics for New Parents Related Articles Birthmarks About Sturge-Weber Syndrome About Facial Paralysis Most Popular Height Predictor - How tall will your kids be? Ideal Body Weight Calculator for Kids and Adults Baby Girl Names Baby Boy Names ... Annoying Questions What's Hot Katrina Relief Annoying Questions Viral Hepatitis Average Weight Woman ... Supplementing Problems adunitCM(150,100,'x55') Sturge-Weber syndrome From Vincent Iannelli, M.D.

37. Sturge-Weber Syndrome sturgeweber syndrome - SWF. The Sturge-Weber Foundation awards the following tosupport projects related to the pathogenesis or treatment of Sturge-Weber http://vpr2.admin.arizona.edu/rso/01080130.htm

STURGE-WEBER SYNDROME - SWF The Sturge-Weber Foundation awards the following to support projects related to the pathogenesis or treatment of Sturge-Weber syndrome and other cerebrovascular syndromes. The awards provide up to $30,000 per year for 2 years. Young Investigator Awards provide postdoctoral support for applicants who received their M.D. or Ph.D. degrees within the past 4 years and will work under an established mentor. Pilot Research Studies are for investigators at any stage of their careers, to support innovative studies with the potential for continued support from other agencies. Contact: Sturge-Weber Foundation, P.O. Box 418, Mount Freedom, NJ 07970. Telephone: (800) 627-5482. Fax: (973) 895-4846. E-mail: swfoffice@aol.com Web: http://www.sturge-weber.com/grants.htm Deadline: 1 March, 1 September 2002. RSO Reference No.:

38. AllRefer Health - Sturge-Weber Syndrome (Encephalotrigeminal Angiomatosis) sturgeweber syndrome (Encephalotrigeminal Angiomatosis) information center coverscauses, prevention, symptoms, diagnosis, treatment, incidence, http://health.allrefer.com/health/sturge-weber-syndrome-info.html

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 Web health.allrefer.com You are here : AllRefer.com Health Sturge-Weber Syndrome Sturge-Weber Syndrome Definition Prevention Treatment Expectations or Prognosis ... Go To Main Page Alternate Names : Encephalotrigeminal Angiomatosis Definition 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. Sturge-Weber Syndrome - Legs Sturge-Weber Syndrome - Soles of Feet Circulatory System The cause of Sturge-Weber is unknown. There is no known hereditary component. Previous Top Next Jump to another section Definition Prevention Treatment Prognosis ... Calling Your Health Care Provider Topics that might be of interest to you Glaucoma Port-Wine Stain Tonometry Other Topics Blindness Laser Therapy Muscle Function Loss Seizures ... Vision Problems Review Date : 11/4/2003 Reviewed By : Celeste Krauss, M.D., Board Certified Clinical Genetics, Clinical Cytogenetics and Pediatrics. Founding Fellow, American College of Medical Genetics. Review provided by VeriMed Healthcare Network.

39. AllRefer Health - Sturge-Weber Syndrome - Soles Of Feet (Pictures, Images, Photo Related Images. • Circulatory System • sturgeweber syndrome - Legs • Sturge-WeberSyndrome - Soles of Feet. Related Articles. • sturge-weber syndrome http://health.allrefer.com/pictures-images/sturge-weber-syndrome-soles-of-feet.h

AllRefer Channels :: Yellow Pages Reference Health Home ... Medical Encyclopedia Web health.allrefer.com You are here : AllRefer.com Health 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. Related Images Circulatory System Sturge-Weber Syndrome - Legs Sturge-Weber Syndrome - Soles of Feet Related Articles Sturge-Weber Syndrome Review Date : 12/9/2001 Reviewed By : A.D.A.M. Medical Illustration Team From Our Sponsors: A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org). URAC's accreditation program is the first of its kind, requiring compliance with 53 standards of quality and accountability, verified by independent audit. A.D.A.M. is among the first to achieve this important distinction for online health information and services. Learn more about A.D.A.M.'s editorial reviewers . A.D.A.M. is also a founding member of Hi-Ethics (www.hiethics.com) and subscribes to the principles of the Health on the Net Foundation (www.hon.ch). Par Web Solutions Health Topics: A-Al Am-Az B C-Cj ... Healthopedia.com

40. Kprones SturgeWeberID10074 Reports exist of tumors found in association with sturgeweber syndrome; Increased fibronectin expression in sturge-weber syndrome fibroblasts and brain http://www.infobiogen.fr/services/chromcancer/Kprones/SturgeWeberID10074.html

Atlas of Genetics and Cytogenetics in Oncology and Haematology Home Genes Leukemias Solid Tumours ... NA Sturge Weber Syndrome Identity Other names Encephalotrigeminal angiomatosis Angio-encephalo-cutaneous syndrome Inheritance Sporadic, equal frequency in the sexes Clinics Phenotype and clinics Sturge Weber Syndrome is a congenital condition characterized by an intracranial vascular anomaly, leptomeningeal angiomatosis, most often involving the occipital and parietal lobes. The anomaly can affect both cerebral hemispheres. An ipsilateral facial cutaneous capillary vascular malformation usually affects the upper face in the V1 distribution of the trigeminal nerve. Other findings include glaucoma, buphthalmos, enlargement of the choriod plexus and seizures. Hemiparesis, hemiatrophy, hemianopia and strokelike events may occur contralateral to the cortical abnormality. Venous stasis results in ischemia underlying the leptomeningeal angiomatosis leading to calcification and laminar cortical necrosis. Skull x-ray film may show classic "tram-line" or "tram-track" calcifications. CT scan may show brain atrophy, calcification and ipsilateral choroid plexus enlargement.

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