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Macrocephaly is a condition in which circumference of the human head is abnormally large. [1] It may be pathological or harmless, and can be a familial genetic characteristic. . People diagnosed with macrocephaly will receive further medical tests to determine whether the syndrome is accompanied by particular disorde
A central nervous system tumor (CNS tumor) is an abnormal growth of cells from the tissues of the brain or spinal cord. [1] CNS tumor is a generic term encompassing over 120 distinct tumor types. [2] Common symptoms of CNS tumors include vomiting, headache, changes in vision, nausea, and seizures. [3]
The human brain is the central organ of the nervous system, and with the spinal cord, comprises the central nervous system. It consists of the cerebrum, the brainstem and the cerebellum. The brain controls most of the activities of the body, processing, integrating, and coordinating the information it receives from the sensory nervous system ...
A cerebral AVM is an abnormal anastomosis (connection) between the arteries and veins in the brain due to the lack of a capillary bed, and are most commonly of prenatal origin. [ 10 ] [ 11 ] In normal cerebral circulation , oxygen-enriched blood from the heart travels in sequence through smaller blood vessels going from arteries, to arterioles ...
Symptoms of AVMs vary according to their location. Most neurological AVMs produce few to no symptoms.Often the malformation is discovered as part of an autopsy or during treatment of an unrelated disorder (an "incidental finding"); in rare cases, its expansion or a micro-bleed from an AVM in the brain can cause epilepsy, neurological deficit, or pain.
A cavernoma in the brain is called a cerebral cavernous malformation or CCM. Despite its designation as a hemangioma, a cavernous hemangioma is a benign (but not harmless) condition, not a malignant tumor, as it does not display endothelial hyperplasia. The abnormal tissue causes a slowing of blood flow through the cavities, or "caverns".
The primary failure is the absence of growth of the brain, rendering the sutures of the cranial vault useless. [17] As a consequence, the sutures close, presenting a pansynostosis like image. [ 17 ] A differentiation between these two conditions can be made with a computed tomography (CT) scan.
Primary familial brain calcification [1] (PFBC), also known as familial idiopathic basal ganglia calcification (FIBGC) and Fahr's disease, [1] is a rare, [2] genetically dominant or recessive, inherited neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement.