Moyamoya disease, an extremely rare disease (one in two million in USA) causing a progressive narrowing of the internal carotid arteries carrying blood to the brain and often resulting in disabling strokes can be successfully treated by a Stanford University neurosurgeon. The disease was first characterized in Japan where moyamoya means puff of smoke and is characterized by a wispy cloud of narrowing blood vessels appearing on X-ray images. The key to successful outcomes is knowing to look for this diagnosis in patients exhibiting otherwise unexplainable symptoms; unexplainable strokes, temporary speech or vision problems, headaches, mental decline, seizures, or attacks of limb numbness and weakness. Most patients are diagnosed as children from 5 to 15, or adults from 30 to 40, and nearly two-thirds are female.
New York Times . Moyamoya.com internet support