This fluid is known as cerebro-spinal fluid and it normally flows from the brain, down the spinal cord and into the bloodstream. If any of the pathways are blocked, the fluid accumulates in the brain, causing it to swell. In babies and infants this causes the head to enlarge, but in older children the bones of the skull are fused and the head size cannot increase, which creates increasing pressure. Usually, a child with hydrocephalus has a shunt surgically inserted and this will drain the fluid and reduce the pressure from day to day.
Hydrocephalus can be present at birth or it can develop following a premature birth. Most children with spina bifida suffer from hydrocephalus. Hydrocephalus can also develop following meningitis, a stroke, a brain haemorrhage or a brain tumour.
Children with hydrocephalus can have fits, but these are not usually directly a result of the hydrocephalus, but rather of the condition which caused the pathways to become blocked. A child with hydrocephalus is likely to have learning difficulties or physical effects. This will vary from child to child and may be very slight.
Key characteristics
A child with hydrocephalus may:
Although a shunt usually works without any problems and is intended to last for a lifetime, it may possibly develop a blockage or an infection, or the tube may require surgically lengthening as the child grows. It is important to notice any sudden changes and to notify the parents straight away, or call the doctor or an ambulance if you feel particularly concerned. Signs
of a blocked or infected shunt are:
Support strategies
You may need to:
Support agencies
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