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Sturge Weber Syndrome - Papers Online

Sturge Weber Syndrome


The is a common, but unknown syndrome that
has no cure but can be treated. The syndrome is usually known at birth by
the presence of a birthmark, and is most often not fatal.
One with the usually encounters seizures at a
very young age. There are many signs such as a port-wine stain that is
noticeable at birth and is consisted of a capillary malformation around the
eye on one side of the face. Abnormal intelligence is usually associated
with the functions of the brain opposite the port-wine stain. Another sign
is Glaucoma which usually developed later on in life for the victims of the
Sturge Weber Syndrome.
The origin to this relentless syndrome is really unknown, Most
doctors who ...

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The patients with the Sturge Weber Syndrome are usually only
impaired on one side of their physique. They experience slow reflexes or
the inability to even move a limb opposite the port-wine stain.
Retardation is by far the worst of all effects. Most do not endure
retardation, but in some causes the extent has been ghastly. On an average
40% of the underprivileged suffering from the Sturge Weber Syndrome has
some degree of retardation. Glaucoma effects only 30% of the patient, but
usually is restricted to on eye and, occurs in later years of their lives.
A port-wine stain is another effect that is on the side of the face even
before birth. It is very noticeable and is applied to almost every patient
with the Sturge Weber Syndrome, but in very rare cases the port-wine stain,
also known as cutaneous hemangioma, is absent. The stain varies in color
from light pink to dark purplish-red, and tends to get darker in time.
Patients also develop epilepsy (also known as a seizure disorder). ...

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by drugs. In most situations surgeons
are hesitant to operate in such a risky procedure. For epilepsy drugs are
used to relieve the harshness, but their is a radical new process. Doctors
from Beth Israel Deaconess Medical Center in Boston have transplanted about
half a million fetal pig brain cells (about the si ze of two droplets of
water) into the brain of a middle-aged man who has severe epilepsy. This is
the first time such a transplant has been tried to treat epilepsy, although
similar pig-to-person brain cell transplants have been tried on people
suffering from Parkinson's disease and Huntington's disease. The hope is
that the pig brain cells will survive, make ...

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Sturge Weber Syndrome. (2005, March 29). Retrieved December 23, 2024, from http://www.essayworld.com/essays/Sturge-Weber-Syndrome/24456
"Sturge Weber Syndrome." Essayworld.com. Essayworld.com, 29 Mar. 2005. Web. 23 Dec. 2024. <http://www.essayworld.com/essays/Sturge-Weber-Syndrome/24456>
"Sturge Weber Syndrome." Essayworld.com. March 29, 2005. Accessed December 23, 2024. http://www.essayworld.com/essays/Sturge-Weber-Syndrome/24456.
"Sturge Weber Syndrome." Essayworld.com. March 29, 2005. Accessed December 23, 2024. http://www.essayworld.com/essays/Sturge-Weber-Syndrome/24456.
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PAPER DETAILS
Added: 3/29/2005 12:42:44 AM
Category: Health & Medicine
Type: Premium Paper
Words: 1324
Pages: 5

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