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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

41. Neurocutaneous Syndromes
sturgeweber syndrome sturge-weber syndrome is a rare condition that affects the skin and the brain. It is caused by a spontaneous
http://kidshealth.org/parent/system/ill/neurocutaneous_p3.html

KidsHealth
Parents Caring for a Seriously or Chronically Ill Child
Tuberous Sclerosis
Tuberous sclerosis is a disorder that causes benign growths, called "tubers," to form on several different organs within the body, including the brain, eyes, kidneys, heart, skin, and lungs. It occurs in approximately one in 6,000 births. There is a 50% chance that a parent with TS will have a child with the disease. The condition is often first recognized in children who experience epileptic seizures or who exhibit developmental delays. The severity of TS varies from mild skin abnormalities to very severe cases that cause mental retardation or kidney failure Treatment usually includes medication to prevent seizures, treatments to address skin problems, surgery to remove tumors (to reduce the risk of cancer as well as for cosmetic reasons), and the management of high blood pressure caused by kidney disease. As with all of the neurocutaneous syndromes, a child's prognosis depends on the severity of the case. Sturge-Weber Syndrome
Sturge-Weber syndrome is a rare condition that affects the skin and the brain. It is caused by a spontaneous genetic mutation and is not passed down by parents who carry the disease. How often it occurs in babies is not known, and because it is not frequently diagnosed, it is difficult to estimate how many people currently have the disease.

42. IRSC - Rare Disorders, Sturge-Weber Syndrome
Rare Disorders sturgeweber syndrome. IRSC Home Rare Disorders sturge-weber syndrome. Categories.
http://www.irsc.org:8080/irsc/irscmain.nsf/sub?readform&cat=Rare Disorders&subca

43. Genetic Disorders, Sturge-Weber Syndrome
Submit Your Site to the sturgeweber syndrome category. Sponsored sturge-weber syndrome Sites. Submit Your Site to the sturge-weber syndrome category.
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  • NORD: Sturge Weber Syndrome - Offers a list of synonyms, a general discussion and further resources.
  • Pediatric Database - A definition of Sturge-Weber syndrome, the epidemiology, pathogenesis, pathology, clinical features, investigations and management.

44. Sturge-Weber Syndrome: XtraMSN Health
2004. A to Z Conditions. sturgeweber syndrome Health24 sturge-weber syndrome is also called Encephalotrigeminal Angiomatosis. It
http://www.xtramsn.co.nz/health/0,,8065-1670066,00.html
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Thu 03 June 2004 A to Z Conditions Sturge-Weber Syndrome
  • Sturge-Weber syndrome is also called Encephalotrigeminal Angiomatosis.
  • It is a congenital disorder characterised by a vascular birthmark and neurological abnormalities.
  • Symptoms of the disorder, which vary widely among patients, may include eye and internal organ irregularities.
  • The most apparent symptom is a facial birthmark or port wine stain which is present at birth and usually involves at least one upper eyelid and the forehead.

45. Sturge-Weber Syndrome
Chapter 1. The Essentials on sturgeweber syndrome Guidelines. Overview. What Is sturge-weber syndrome? sturge weber syndrome. foundation sturge weber.
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

46. Conditions And Diseases - Sturge-Weber Syndrome Top Links
sturgeweber syndrome Web Site Links. Stephie s Corner - A mother s journal of her daughter s life with Sturge - Weber syndrome.
http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Genetic_Diso
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Related Healthcare Subjects Disabilities Environmental Health Fitness Health Insurance ... Men's Health
Sturge-Weber Syndrome Web Site Links Stephie's Corner A mother's journal of her daughter's life with Sturge - Weber syndrome. The site highlights the personal aspects of the syndrome and how it affects daily life.
The Sturge-Weber Foundation
A support site for individuals and professionals dealing with Sturge-Weber syndrome, port-wine stains and Klippel Trenaunay. The Foundation acts as clearing house for information and a focus for research.
NORD - Sturge Weber Syndrome
Offers a list of synonyms, a general discussion and further resources.
Pediatric Database
A definition of Sturge-Weber syndrome, the epidemiology, pathogenesis, pathology, clinical features, investigations and management.
Other Useful Health Web Links National Institutes of Health (NIH) US Government department in charge of medical research.
AHRQ: Clinical Information
Clinical information on evidence-based practice, clinical guidelines, medical effectiveness, pharmaceutical therapy, new technology, screening and preventive services, outcomes research, and the National Guideline Clearinghouse.
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47. Children's Hospital & Health System - Sturge-Weber Syndrome
sturgeweber syndrome. The first most obvious sign of sturge-weber syndrome is a baby born with a facial birthmark. It usually will
http://www.chw.org/display/PPF/DocID/8486/router.asp
Sturge-Weber Syndrome
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Programs and Clinics Programs and Clinics ... Vascular Malformations : Sturge-Weber Syndrome E-mail this page Print this page
Sturge-Weber Syndrome
The first most obvious sign of Sturge-Weber syndrome is a baby born with a facial birthmark. It usually will cover at least one eyelid and the forehead. The stain will vary in color and size. In rare cases, there is no port wine stain. Neurological problems are caused by excessive blood vessel growth on the surface of the brain. Seizures are the most common early problem, often starting by 1 year of age. Developmental delay also may occur in varying degrees. Other problems may affect:
Eyes - Increased pressure within the eye (glaucoma) can also be present at birth or develop later. This affects about 30 percent of patients with Sturge-Weber. It most often affects the eye with the port wine stain. Organs - Other body organs can be affected, although this is rare. Back to top Report any problems or comments about this Web site to Webmaster@chw.org

48. Sturge Weber Syndrome
Sturge Weber Syndrome. A congenital Each case of sturgeweber syndrome is unique and exhibits findings to varying degrees. The most
http://www.cv.quik.com.au/hmegroup/Aust/Sturge Weber.htm
Sturge Weber Syndrome
A congenital facial birthmark and neurological abnormalities characterize this condition. Other symptoms associated can include eye and internal organ irregularities. Each case of Sturge-Weber syndrome is unique and exhibits findings to varying degrees. The most apparent indication of Sturge-Weber syndrome is a facial birthmark or "port wine stain" present at birth and typically involving at least one upper eyelid and the forehead. Neurological concerns relate to the development of excessive blood vessel growth on the surface of the brain (angiomas). Seizure activity is the most common early problem, often starting by one year of age. The convulsions usually appear on the opposite side of the body from the port wine stain and vary in severity. A weakening or loss of the use of one side of the body may develop opposite to the port wine stain. Developmental delay of motor and cognitive skills may also occur to varying degrees. Australian Sturge Weber Support Group Emedicine - Sturge Weber Page Contact A Family UK - Sturge Weber Page

49. Sturge-Weber Syndrome
Selected medical images OMIM sturgeweber syndrome. CT and MR patterns of sturge-weber syndrome; Lecture 23 Adrenal gland; Sturge-Weber;
http://www.gfmer.ch/Genetic_diseases/Sturge-Weber_syndrome/Sturge-Weber_syndrome
Selected medical images
OMIM

Sturge-Weber syndrome Sources
Print this page
Edited by Aldo Campana, August 13, 2003

50. STURGE-WEBER SYNDROME
Features Listed For sturgeweber syndrome. McKusick 185300. Advanced tooth eruption/development; Buphthalmos; Capillary haemangioma; Cavernous haemangioma;
http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?1646

51. 24Dr.com Reference Library - Encyclopaedia - Sturge-Weber Syndrome
sturgeweber syndrome. What is it? Sturge-Weber is a condition which consists of a birth mark always involving the forehead and a
http://www.24dr.com/reference/encyclopaedia/sturge_weber.htm
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STURGE-WEBER SYNDROME
What is it?
Sturge-Weber is a condition which consists of a birth mark always involving the forehead and a similar blood vessel abnormality on the brain surface (often called an angioma). Sometimes the birth mark may be on one side only, sometimes it is on both sides. Occasionally it may also be on the trunk or limbs, again on one or both sides. By some process which probably involves depriving the underlying brain of some of its blood supply, the underlying brain shrinks, and specks of calcium appear in it. This process probably also causes the brain angioma to grow over the surface of the brain usually from the back towards the front.
Who gets it?
It is probably not hereditary. If a first child has it, the chances of further children having it are less than one in a hundred. There are cases on record of each in a pair of identical twins having it, and also of only one in a pair having it. There is also one record of both the father and the son having it but this is so rare that it is probably a coincidence. It seems that the hitch in blood vessel development is an accident of nature. Nothing that happens or does not happen in pregnancy seems to cause it.
What are the symptoms?

52. Sturge Weber Syndrome,Dimitri Disease,Encephalofacial Angiomatosis,Encephalotrig
sturgeweber syndrome also known as Leptomeningeal Angiomatosis Dimitri Disease Encephalofacial Angiomatosis Encephalotrigeminal Angiomatosis Meningeal
http://www.icomm.ca/geneinfo/sturge.htm
Sturge Weber Syndrome,Dimitri Disease,Encephalofacial Angiomatosis,Encephalotrigeminal Angiomatosis,Leptomeningeal Angiomatosis,Meningeal Capillary Angiomatosis,Sturge-Kalischer-Weber Syndrome,Sturge-Weber Phakomatosis,SWS,Sturge Weber Syndrome,Dimitri Disease Encephalofacial Angiomatosis,Encephalotrigeminal Angiomatosis,Leptomeningeal Angiomatosis,Meningeal Capillary Angiomatosis,Sturge-Kalischer-Weber Syndrome,Sturge-Weber Phakomatosis,SWS
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DISORDERS GLOSSARY Sturge-Weber Syndrome
also known as:
Leptomeningeal Angiomatosis
Dimitri Disease
Encephalofacial Angiomatosis
Encephalotrigeminal Angiomatosis
Meningeal Capillary Angiomatosis Sturge-Kalischer-Weber Syndrome Sturge-Weber Phakomatosis SWS (as defined by the National Organization for Rare Disorders
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.

53. Genetic Disorders: Sturge-Weber Syndrome
Genetic Disorders sturgeweber syndrome. NORD Sturge Weber Syndrome. Offers a list investigations and management. sturge-weber syndrome Community.
http://www.puredirectory.com/Health/Conditions-and-Diseases/Genetic-Disorders/St
Genetic Disorders: Sturge-Weber Syndrome
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Standard Listings
NORD: Sturge Weber Syndrome
Offers a list of synonyms, a general discussion and further resources.
Pediatric Database
A definition of Sturge-Weber syndrome, the epidemiology, pathogenesis, pathology, clinical features, investigations and management.
Sturge-Weber Syndrome Community
Support group for individuals and families affected by SWS.
The Sturge-Weber Foundation
A support site for individuals and professionals dealing with Sturge-Weber syndrome, port-wine stains and Klippel Trenaunay. The Foundation acts a...
Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor PureDirectory.com uses a modified version of the Open Directory.

54. Wills Glaucoma Service & Foundation: ICE Syndrome, Sturge-Weber Syndrome, Inflam
ICE Syndrome, sturgeweber syndrome, Inflammatory Traumatic Glaucoma Chat Highlights December 12, 2001. P What causes sturge-weber syndrome?
http://www.wills-glaucoma.org/supportgroup/20011212.html

Chat Highlights
December 12, 2001
Norma Devine, Editor
On Wednesday, December 12, 2001, Dr. Rick Wilson
Moderator:
Doctor Rick, tonight we would like to discuss four types of glaucoma: Iridocorneal endothelial (ICE) syndrome, Sturge-Weber syndrome, inflammatory glaucoma, and traumatic glaucoma. What do these types of glaucoma have in common? Dr. Rick Wilson: They are all secondary glaucomas, caused by a visible problem, as opposed to chronic open-angle glaucoma, the cause of which is unknown. In ICE, a spectrum of diseased corneal endothelium, the inside lining of the cornea, grows off the cornea, covers the drain or pulls the iris up over the drain, blocking it. The cornea is injured by this abnormal lining and often gets swollen at a lower-than-usual intraocular pressure. Moderator: What causes ICE? Dr. Rick Wilson: ICE may result from a herpes simplex infection of the cornea in utero (before birth). P: At what age does ICE commonly occur? Is it unilateral? Dr. Rick Wilson:

55. Sturge-Weber Syndrome
sturgeweber syndrome Chandru Krishnan, MD Tufts University School of Medicine New England Eye Center Boston, MA. Mandar M. Joshi
http://www.ophthalmic.hyperguides.com/Tutorials/glaucoma/Sturge_Weber_Syndrome/d
You've spent minutes on Ophthalmic Hyperguide Sturge-Weber Syndrome
Chandru Krishnan, MD
Tufts University School of Medicine
New England Eye Center
Boston, MA Mandar M. Joshi, MD
New England Eye Center
Boston, MA

56. Sturge-Weber Syndrome And The Eye
sturgeweber syndrome and the Eye. Chandru Krishnan, MD Mandar Joshi, MD. Approximately 30% to 40% of patients with sturge-weber syndrome have glaucoma.
http://www.ophthalmic.hyperguides.com/Tutorials/glaucoma/Sturge_Weber_Syndrome/t
You've spent minutes on Ophthalmic Hyperguide
Sturge-Weber Syndrome and the Eye Chandru Krishnan, MD
Mandar Joshi, MD
Introduction
Sturge-Weber syndrome is one of several syndromes classified under the heading of phakomatosis because it involves pathology in the skin, eye, and brain. The first reported description of Sturge-Weber syndrome associated with eye involvement has been attributed to Schirmer in 1860. He reported a patient with facial nevus flammeus and ipsilateral buphthalmos. Sturge later reported on a patient who had these findings, along with neurologic findings, and proposed that there were vascular abnormalities in the brain and eye along with the skin. Weber verified neurologic involvement radiologically. Inheritance of disease is sporadic and eye involvement is almost exclusively unilateral. It is believed that men and women are equally affected. Histopathology is significant for hamartomatous malformation of cephalic blood vessels causing hemangiomas of the skin, meninges, and eye. A layer of endothelium lines these dilated blood vessels. Typically, the lesions remain constant throughout life. Calcification of brain tissues adjacent to hemangiomas causes seizures, mental retardation, hemiparesis, and hemianopia. The facial lesion (port-wine stain) occurs along a distribution similar to the branches of the trigeminal nerve. However, the hemangioma often traverses the midline ( Slide 1 Slide 1 Ocular manifestations include choroidal, episcleral, and conjunctival hemangiomas, glaucoma, and heterochromia of the iris

57. :: Ez2Find :: Sturge-Weber Syndrome
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58. Sturge-Weber Syndrome
What is sturgeweber syndrome? Information from the British Epilepsy Associaion. Outcome of sturge-weber syndrome in 52 adults (abstract). Link Lists.
http://www.nhbvi.com/internet/Eye/sturge-weber.html
Search:
What is Sturge-Weber Syndrome? Information from the British Epilepsy Associaion Information from Contact a Family Information from the Medical College of Wisconsin Information from the National Institute of Neurological Disorders and Stroke ... Information from SpecialChild.com
Discussion, Publications, and Support
Sturge-Weber Foundation Sturge-Weber Foundation (UK) Sturge-Weber Support Group of New Zealand Sturge-Weber_Syndrome Listserv at Yahoo! Groups ... SWFYA Listserv at Yahoo! Groups
Research and Treatment
"Outcome of Sturge-Weber syndrome in 52 adults" (abstract)
Link Lists
Family Village Links from Stephie's Corner Yahoo!
Personal Web Pages
Breezy's Page Jordon's Story Nicole's Page Our Daily Lives with SWS ... Stephie's Corner

59. Your Healthcare Primer For Long Term Care: Sturge-Weber Syndrome. UNM Health Sci
sturgeweber syndrome. Definition. sturge-weber syndrome is a neurocutaneous (brain-skin) disorder characterized by three features
http://star.nm.org/manual/sturge-weber/
UNM COC : Your Healthcare Primer for Long Term Care

Sturge-Weber Syndrome
Definition
Sturge-Weber Syndrome is a neurocutaneous (brain-skin) disorder characterized by three features:
  • Port wine stain (cutaneous facial angioma) Seizures and other neurologic complications associated with angioma of the leptomeningies Glaucoma (increased pressure within the eyeball.)
  • Introduction
    Sturge-Weber Syndrome (also called encephalotrigeminal angiomatosis) is an uncommon condition. It occurs in 1:50,000 to 1:60,000 births. The cause is unknown but some scientists think it is the result of abnormal development of the primordial vascular bed (blood supply) of the brain very early in the formation of the embryo. Most cases are sporadic but occasionally cases within families are reported. Males and females seem to be equally affected. It has been reported in individuals of White, Hispanic, African and Asian heritage. The facial port wine stain is present at birth in 98% of individuals with Sturge Weber Syndrome. In general the port wine stain tends to be found in the area of the face enervated by the fifth cranial nerve (trigeminal nerve.) It tends to be unilateral (on one side or the other) but can be bilateral (on both sides.) Port wine stain may also be found on the trunk or extremities of some individuals with Sturge Weber Syndrome. Not all individuals with port wine stain have Sturge Weber.

    60. Sturge-Weber Syndrome
    The New Health Directory, Directory, Home Health Conditions and Diseases Genetic Disorders sturgeweber syndrome (3) See Also
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    Directory Home Health Conditions and Diseases Genetic Disorders : Sturge-Weber Syndrome (3)
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