Search results
Results From The WOW.Com Content Network
Hydrocephalus can be classified via mechanism into communicating, noncommunicating, ex vacuo, and normal pressure hydrocephalus. Diagnosis is made by physical examination and medical imaging, such as a CT scan. [1] Hydrocephalus is typically treated through surgery. One option is the placement of a shunt system. [1]
Macewen's sign or Macewen sign (/ m ə ˈ k j uː ə n / mə-KEW-ən) is a sign used to help to diagnose hydrocephalus [1] (accumulation of excess cerebrospinal fluid) and brain abscesses. Tapping the skull near the junction of the frontal, temporal, and parietal bones will produce cracked pot sound. Positive test is indication of separated ...
Gait symptoms improve in ≥ 85% patients. Cognitive symptoms improve in up to 80% of patients when surgery is performed early in the disease course. Urgency and incontinence improve in up to 80% of patients, but only in ≤ 50–60% of patients with shunt implanted late in disease course.
Blockage of the aqueduct can lead to hydrocephalus, specifically as a common cause of congenital and/or obstructive hydrocephalus. [ 1 ] [ 2 ] The aqueduct of Sylvius is the channel which connects the third ventricle to the fourth ventricle and is the narrowest part of the CSF pathway with a mean cross-sectional area of 0.5 mm 2 in children and ...
Low-pressure hydrocephalus (LPH) is a condition whereby ventricles are enlarged and the individual experiences severe dementia, inability to walk, and incontinence – despite very low intracranial pressure (ICP). [1] Low pressure hydrocephalus appears to be a more acute form of normal pressure hydrocephalus. If not diagnosed in a timely ...
Craniosynostosis occurs when the sutures of the skull close too early. The result of multiple sutures fusing before the brain stops growing is an increase in ICP leading to hydrocephalus. [17] 0.05% [18] Post-meningitic hydrocephalus The inflammation and scarring caused by meningitis can inhibit CSF absorption. Dandy–Walker syndrome
L1 syndrome is a group of mild to severe X-linked recessive disorders that share a common genetic basis. The spectrum of L1 syndrome disorders includes X-linked complicated corpus callosum dysgenesis, spastic paraplegia 1, MASA syndrome, and X-linked hydrocephalus with stenosis of the aqueduct of Sylvius (HSAS).
These include hydrocephalus, cerebellar tonsillar herniation , seizures and syringomyelia. These complications are not usually congenital, they develop over time often presenting complications in late infancy or early childhood, though they can become problems even later.