Doctor insights on:
Parkes Weber Syndrome
Klippel-Trenaunay-Weber Syndrome: Klippel-Trenaunay-Weber Syndrome is a rare vascular congenital condition due to improper formation of blood and/or lymphatic vessels. It has three features: Port Wine Stain (nevus flammeus or capillary hemangioma), venous or/and lymphatic malformations, and enlargement (soft-tissue hypertrophy) of the affected extremity. ...Read more
Blood vessel malform: Rare congenital medical condition in which blood vessels and/or lymph vessels fail to form properly. The three main features are nevus flammeus (port-wine stain), venous and lymphatic malformations, and soft-tissue hypertrophy of the affected limb. Often called angio-osteohypertrophy or hemangiectatic hypertrophy and is found as a congenital defect at time of birth in many cases. ...Read more
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. ...Read moreSee 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. ...Read moreSee 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. ...Read more
What dr or drs do I see for osler weber rendu syndrome. My ENT dr. Was not very helpful.
Osler Weber Rendu: Owr syndrome is an hereditary problem that causes multiple blood vessel growths called telangectasias. These cause bleeding problems, especially frequent nose bleeds. There is usually a family history of hereditary hemorrhagic telangectasias (hht). Most ENT dr.'s have some experience with this problem but may have exposure to only a few patients. Most academic centers will have hht clinics. ...Read more
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 over ...Read moreSee 1 more doctor answer
My question is my aunt she osler –weber- rendu syndrome my main concern is her nose bleed continuously i'm afraid she will leave us soon is there a ?
Is there a cure?: I think you are asking for treatment of nosebleeds for osler weber rendu.For severe cases, most will use an nd-yag laser (special type of laser) to cauterize the vessels on the septum that are causing the problem. Ask you ENT if he does this or send her to someone who does.Other options involve using a catheter to thread into the feeding vessels to embolism arteries involved. Also septoplasty. ...Read more
Not only those 2: The other name for it is hereditary hemorrhagic telangiectasia, meaning tortuous blood vessels occur in many parts of the body: nose (causing nosebleeds), stomach (bleeding into the gut), skin and moist membranes (spider veins), liver, lungs, and brain or spine (may manifest as ataxia, stroke, seizures or hemorrhage). Get tested for avms at any other sites. Good luck! ...Read more
Yes: The distal (lower end) fibula is also know as the lateral malleolus. The weber classification of ankle fractures classifies based on the location of the fracture (break) with respect to the syndesmosis (connection between tibia and fibula just above the ankle joint. A = below syndesmosis, b = at level, c = above. As you go from a to b to c, the risk of syndesmosis injury increases. ...Read moreSee 3 more doctor answers