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         Sturge-weber Syndrome:     more detail
  1. 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
  2. Sturge-Weber Syndrome: The Resource Guide for a Reason, a Season, and a Lifetime
  3. Sturge-Weber Syndrome
  4. Sturge-Weber Syndrome
  5. Sturge-Weber syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Deepti, MS Babu, 2005
  6. Sturge-Weber syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Deepti, MS Babu, 2005
  7. The Sturge-Weber syndrome by George Lionel Alexander, 1960
  8. Sturge-Weber syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Children's Health: Infancy through Adolescence</i> by Christine Kelly, 2006
  9. Sturge-Weber Syndrome by George Lionel Alexander, R.M. Norman, 1960-12
  10. A fourth type of phakomatosis, Sturge-Weber syndrome, (Verhandelingen der Koninklijke Akademie van Wetenschappen te Amsterdam, Afdeeling Natuurkunde, 2. sect) by Bernard Brouwer, 1937
  11. Neurocutaneous Disorders: Phakomatoses & Hamartoneoplastic Syndromes
  12. Brain involvement in Sturge-Weber.(SPECIAL NEEDS: REALIZING POTENTIAL): An article from: Pediatric News by Anne Comi, 2009-02-01
  13. 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

61. ¥¹¥¿¡¼¥¸¡¦¥¦¥§¡¼¥Ð¡¼¾É¸õ·² Sturge-Weber Syndrome
von HippelLindau?,VHL. · sturge-weber syndrome. ConcisePathology 21, p.910 ,
http://akimichi.homeunix.net/~emile/aki/medical/dermatology/node86.html
Next: ¥¯¥ê¥¥Ú¥ë¡¦¥¦¥§¡¼¥Ð¡¼¾É¸õ·² Klippel-Weber syndrome Up: ÊìÈ¾É phacomatosis Previous: von Hippel-LindauÉÂ,VHL

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62. NCI: Sturge-Weber Syndrome
Numbers A B C D E F G H I J K L M N O P Q R S T U V W X Y Z sturgeweber syndrome. SWS. A rare, congenital disorder that affects the brain, skin, and eyes.
http://www.jamesline.com/patientsandpublic/cancertypes/glossary/index.cfm?action

63. Sturge-Weber Syndrome
SturgeWeber Foundation (UK) Burleigh, 348 Pinhoe Road, Exeter EX4 8AF Tel 01392 464675 support@sturgeweber.org.uk on differents aspects of the syndrome and to
http://www.ion.ucl.ac.uk/library/patient/sturge.htm
Sturge-Weber Syndrome Medline NLM definition: A congenital syndrome characterized by a port-wine nevus covering portions of the face and cranium (in the distribution of the ophthalmic division of the TRIGEMINAL NERVE) and angiomas of the meninges and choroid. Clinical manifestations include the onset of focal SEIZURES, progressive hemiparesis, GLAUCOMA, hemianopsia, and cognitive deficits in the first decade of life. By age two years, skull radiographs reveal "tramline calcifications" of the margins of the occipital and parietal lobes. Pathologically cortical neurons are replaced by glial tissue that undergoes calcification.
Pubmed Medline search on Sturge-Weber Syndrome
Sturge-Weber Syndrome
: National Institute for Neurological Disorders and Stroke
Sturge-Weber Syndrome
: Contact a Family Support Groups Sturge-Weber Foundation
(UK)
Burleigh, 348 Pinhoe Road, Exeter, EX4 8AF
Tel: 01392 464675
support@sturgeweber.org.uk

Aims to provide support and information on differents aspects of the syndrome and to raise both public and professional awareness of the condition. Promotes medical research into the causes and treatment of this syndrome. A Family Weekend is organised every year, usually in October, when doctors and other professionals talk about relevant topics. They publish a newsletter.

64. Sturge-Weber Syndrome - Online Neuropathology Atlas
Sturge Weber - Dimitri Disease (Encephalotrigeminal angiomatosis) Angiomatosis encephalotrigeminalis.
http://www.neuropat.dote.hu/stuge.htm
Sturge -Weber - Dimitri Disease (Encephalotrigeminal angiomatosis)
Angiomatosis encephalotrigeminalis
Naveus flammeus Microscopic appearance
Microscopic appearance

(Click on any image for larger view) Related Internet links var site="sm5hegeduskdote" Last modified: February 17, 2001
If you have any comments, please, contact Neuroanatomy Structures Online Neuropathology Atlas Internet Handbook of Neurology

65. Sturge-Weber Syndrome - Cancer Terms And Definitions By Health Dictionary
sturgeweber syndrome SWS. A rare, congenital disorder that affects the brain, skin, and eyes. Abnormal blood vessel growth occurs
http://www.health-dictionary.com/cancer_term_details/Sturge-Weber_Syndrome
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Sturge-Weber Syndrome:
SWS. A rare, congenital disorder that affects the brain, skin, and eyes. Abnormal blood vessel growth occurs in the trigeminal nerve in the face and the meninges (covering) of the brain. This abnormal growth causes red or purple skin discoloration (sometimes called a port wine stain), usually on one side of the face, and can also cause seizures, learning disabilities, and glaucoma.
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Information and definitions of the medical conditions and diseases have been taken from various reliable government publications and we have done our best to verify their accuracy. If you feel any of the definitions are incorrect or needs to be updated please contact us and we will look into it. Contact Health Dictionary - Medical and Disease Terms and Definitions
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66. Sturge-Weber Syndrome
Search Registration Help Disclaimer. sturgeweber syndrome. Image URL sturge-weber syndrome, Image URL sturge-weber syndrome,
http://www.brisbio.ac.uk/ROADS/subject-listing/sturgewebersyndrome.html
A collection of medical, dental and veterinary images for use in teaching. Home About the Archive FAQ Terms and Conditions ... Help
Sturge-Weber Syndrome
Sturge-Weber syndrome Sturge-Weber syndrome

67. Article : Choroidal Hemangioma With A Bleed In Sturge-Weber Syndrome - MRI ; Aut
LETTER TO EDITOR Choroidal Hemangioma with a bleed in sturgeweber syndrome MRI. Sir,. The sturge-weber syndrome comparison of MR and CT characteristics.
http://www.ijri.org/articles/archives/2003-13-2/letter233.htm
LETTER TO EDITOR
Choroidal Hemangioma with a bleed in Sturge-Weber Syndrome: MRI

Sir, In Sturge-Weber syndrome, common ocular findings include: buphthalmos, choroidal angiomas, and episcleral telangiectasias [1]. Buphthalamos (occurs in 15% of cases) is caused by congenital glaucoma due to increased pressure, which may be related to impaired reabsorption of ocular fluid [1]. In almost one third of the cases either the sclera or the ocular choroid may show a dilated plexus of vessels [1]. These abnormal vessels are immature and have histologic features resembling both dilated capillaries as well as small viens and are often described as telangiectasias [1]. Slit-lamp examination help identify this vascular abnormality. We described the MRI findings in a case of choraidal haemangioma. Fig. 1, Fluid-Attenuated Inversion Recovery, axial image (TR/TE/TI: 5000/ 100/ 1900) shows strongly hyperintense vitreous with a sliver of relatively low signal intensity ill-defined lesion in the choroid and retinal region. Fig. 2, A. Plain T1-weighted axial image (TR/TE: 500/ 25) shows a sliver of soft tissue signal intensity lesion in the choroid. Hyperintense vitreous is consistent with bleed. B. Post contrast image shows intense enhancement of the soft tissue component.

68. Sturge-Weber Syndrome: MRI Findings - Eurorad - Clinical Case 1268 - Resident
Neuroradiology Miscellaneous Case 1268 sturgeweber syndrome MRI findings D. Chourmouzi,G. Boulogianni, A.Drevelegas Diagnosis. sturge-weber syndrome.
http://www.eurorad.org/case.cfm?uid=1268

69. CT And MR Patterns Of Sturge-Weber Syndrome - Eurorad - Clinical Case 1230 - Res
Neuroradiology Miscellaneous Case 1230 CT and MR patterns of sturgeweber syndrome V. Goncalves, P. Schnyder, M. Wintermark Diagnosis. sturge-weber syndrome.
http://www.eurorad.org/case.cfm?uid=1230

70. Disease - Sturge-Weber Syndrome - Hartford, Connecticut , Saint Francis Care
Back to main Health Information page Disease sturge-weber syndrome. Definition sturge-weber syndrome is a rare disorder present at birth.
http://www.saintfranciscare.com/13901.cfm
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Circulatory system
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. Alternative Names: Encephalotrigeminal angiomatosis Causes And Risk: The cause of Sturge-Weber is unknown. There is no known hereditary component. Prevention: There is no known prevention. Symptoms: Signs And Tests: X-rays, MRI, or CT scans are useful to look for associated problems. Treatment:
  • Anticonvulsant medicine for convulsions.

71. DermIS / Main Menu / DOIA / Sturge-Weber Syndrome / Images
DermIS / main menu / DOIA / sturgeweber syndrome / images, deutsch español portugues français. / images for the diagnosis sturge-weber syndrome .
http://dermis.multimedica.de/doia/diagnose.asp?zugr=d&lang=e&diagnr=759610&topic

72. Sturge-Weber Syndrome
sturgeweber syndrome. The association between a port-wine stain on the face and scalp and raised eye pressure - the Sturge-Weber
http://www.iga.org.uk/servlet/dycon/iga/iga/live/en/uk/AboutGlaucoma_OtherEyeCon
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Sturge-Weber Syndrome
The association between a port-wine stain on the face and scalp and raised eye pressure - the Sturge-Weber syndrome is an uncommon one and usually occurs at an early age, although it has occasionally been found to develop insidiously in young adults, or even in later life.
Mild cases can sometimes be controlled by medical treatment (usually eye drops) but in most cases surgery is necessary to improve the drainage of fluid from the eye.
The degree of glaucoma varies considerably from person to person and in these cases and only the eye specialist who has examined the patient can judge what treatment is necessary for that individual.
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73. OMIM - STURGE-WEBER SYNDROME

http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=185300

74. Database Search Results
database does not imply endorsement by the US Department of Health and Human Services.. Searched keywords for sturgeweber syndrome.
http://www.health.gov/nhic/NHICScripts/Hitlist.cfm?Keyword=Sturge-Weber Syndrome

75. Corpus Christi Online - / Sturge-Weber Syndrome Hurts Boy, Family
Thursday, Mar. 25, 1999 sturgeweber syndrome hurts boy, family. `Port wine marks on face just a part of the misery. By SYLVIA R. LONGORIA
http://www.caller.com/autoconv/slongoria99/slongoria22.html
Marketplace Services Contact Us Community ... Local Guides Thursday, Mar. 25, 1999
Sturge-Weber Syndrome hurts boy, family
`Port wine' marks on face just a part of the misery
By SYLVIA R. LONGORIA
Staff Writer
Belinda Gonzalez was devastated when her son, Alex, came home from school crying one day. "The kids had called him names. They wanted to know why he has two colors of skin on his face.
"I was so upset I had to go to another room and cry before I could go back and tell him everything was going to be OK."
Alex, 8, a student at West Oso's JFK Elementary, was diagnosed with Sturge-Weber Syndrome in 1993, a congenital disorder of unknown origin that causes a facial birthmark, or "port wine stain," usually on one side of the face.
Schoolmates have no idea that what Alex has leads to seizures, neurological abnormalities such as glaucoma, and internal organ irregularities. What they do see, however, is a side of his face that turns even deeper in color whenever he engages in physical activity. Which is why they nicknamed him "two face."
The teasing got so bad, Alex said, that he dreaded going to school.

76. PharmGKB: Sturge-Weber Syndrome
sturgeweber syndrome. Alternate Names Angiomatoses, Meningo-Oculo-Facial; Angiomatosis Oculoorbital-Thalamic Syndrome; Angiomatosis
http://www.pharmgkb.org/do/serve?objId=PA445756&objCls=Disease

77. OSL: Sturge-Weber Syndrome With Bilateral Congenital Syndactyly - A Previously U
Volume 30 (3) * March 1999 * Case Reports (abstract). sturgeweber syndrome With Bilateral Congenital Syndactyly A Previously Undescribed Association.
http://www.slackinc.com/eye/os/stor0399/mandal.htm
Ophthalmic Surgery and Lasers
[About Ophthalmic Surgery and Lasers [Table of Contents]
Volume 30 (3) * March 1999 * Case Reports (abstract)
Sturge-Weber Syndrome With Bilateral Congenital Syndactyly:
A Previously Undescribed Association
Anil K. Mandal, MD
ABSTRACT
The Sturge-Weber syndrome consists of unilateral port-wine haemangioma of the face which may be associated with an ipsilateral intracranial haemangioma and choroidal angioma. The common derivation of the meningeal, choroidal and facial vessels may explain a congenital malformation of all three areas. I report the case of a child with typical Sturge-Weber syndrome who had a previously undescribed association with bilateral congenital syndactyly.
Ophthalmic Surg and Lasers
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Accepted for publication October 13, 1998.
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78. Sturge-Weber Syndrome
sturgeweber syndrome - SWF. The Sturge-Weber Foundation awards the following to support projects related to the pathogenesis or
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.:

79. Alexa Web Search - Subjects > Health > Conditions And Diseases > Genetic Disorde
sturgeweber syndrome Subjects Health Conditions and Diseases Genetic Disorders sturge-weber syndrome. Bestselling Products in sturge-weber syndrome.
http://www.alexa.com/browse/general?catid=551850&mode=general

80. Healthfinder® - Sturge-Weber Syndrome
sturgeweber syndrome A general overview of sturge-weber syndrome that includes a description of the disorder, treatment, prognosis and research information.
http://www.healthfinder.gov/Scripts/SearchContext.asp?topic=826

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