Doctor insights on:
Sturge Weber Syndrome Life Expectancy
See below: Sturge-weber syndrome is a rare disorder that is present at birth. A child with this condition will have a port-wine stain birthmark (usually on the face) and nervous system problems. The cause of sturge-weber is unknown.
Genetic cause is: Usually sporadic, possibly due to mosaicism-some, but not all cells have gene abnormalities. Eeg's to look for seizures (~ 70%). Neuromaging to monitor growth of hemangiomas, blood vessel abnormalities of brain & brain coverings. Vision exams for glaucoma (30-48%) & hemianopia (decreased vision in one eye). Iq tests for intellectual disability (~40%).See http://www. Sturge-weber. Org/resources/about.See 1 more doctor answer
Can include:: Medical management of seizures, laser surgery for port-wine stain, possible brain surgery for intracranial hemangiomas, ophthalmological treatment of glaucomas & follow-up of hemianopia (decreased vision of one eye) physical therapy for hemiplegia (weakness of one side), early intervention fordevelopmental delays, special education supports for intellectual disability, behavioral therapy.See 1 more doctor answer
Vascular anomaly: Children were described by sturge and weber who had port wine stain on the face and vascular anomaly in the brain. Often with severe epilepsy and cerebral palsy, there is no cure. Management involves treating seizures, glaucoma, and their frequent headaches. Brain surgery can be offered in severe cases. Lazer treatments may help the face lesion.
Hard to say: Since you didn't provide enough background information, I cannot say. You did not provide information about the location of this stain, which is very important. You did not indicate other features of the problem. The site is not a chat room. The questions are not linked. Each question must have the basic information needed to describe the issue before an answer can be formulated. Please start overSee 1 more doctor answer
Normal: Life expectancy should be normal. There are no effects that affect heart, or other major systems that would reduce life expectancy.
May be normal: Children with Noonan's Syndrome may have cardiac abnormalities such as pulmonic stenosis, ASD (atrial septal defect), VSD (ventricular septal defect). If these abnormalities are mild, then the life expectancy may be normal.
Williams syndrome: Check out this site: http://williams-syndrome. Org/ws.Get a more detailed answer ›
Prognosis in West: Syndrome depends on having an identifiable prenatal, perinatal, postnatal or unknown cause, developmental status & neurological findings at time of presentation & results of neuroimaging, molecular genetic & metabolic testing. Contact Dr. Mohammad Mahdi Taghdiri, Mofid Hospital, en. Mch. Sbmu. Ac.ir or Dr.. Gholamreza Zamani Ghaletaki, tums (calcium carbonate).ac. Ir/faculties/zamanigh.See 2 more doctor answers
Genetic disorder: Rare disorder multiple systems involved apearance of face and body demonstrates poor developement. Loss of hearing, diabetes, heart failure, aortic valve abnormalities, high blood pressure, just to name a few issues. Life expectancy depends on early diagnosis and intense treatment and follow up. It can be normal except if there heart defect that is serious.
Here are some...: Since West syndrome is a very rare epileptic condition in the infants, most of doctors may not have personal experience in it. But, I found the contents in the link to follow could be helpful; that is http://syndrome. Org/west-syndrome/. Best wish to his health and your family; Happy Holidays 2015.
Depends: On the course of the disease, organ involvement, baseline health status, the aggressiveness of the condition, and many other factors (response to treatment, etc.).
Genetic disorders: It would help if you would be specific about what your genetic disorder is.
Unknown: It is not known if FAS affects life expectancy.
Several treatments!: Yes! children and adults with marfan syndrome can have gradual widening of the aorta - the major artery connected to your heart. Sometimes the aorta becomes so weak that it breaks. But your cardiologist can use an ultrasound machine to watch your aorta very carefully. She can treat you with medicines to slow down the enlargement, and your chest surgeon can even replace your aorta if necessary.See 1 more doctor answer
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