What is hydramentphalia?

hydramentphalia is congenital (present at birth) that devastates and fatal for children for parents. When this happens, most of the brain, including all or most brains of the brain, did not develop. Instead, brain hemispheres are replaced by liquid. There is some brain function, which means that some infants are not immediately diagnosed, but over time, usually within a month or two, the development of symptoms associated with hydramentphali cannot be ignored.

There are a number of things that can be risk factors for the fetus developing this condition. Many in a pregnant mother may be among the highest. Sometimes the death of twins in the uterus increases the risk. Drug abuse could lead to unsuccessful brain development. Other medical literature points to exposure to certain diseases. It is clear that there is no single definable cause.

The symptoms of hydramentphalia can also be variable. In some infants, enough bra function is present for children to initially appear quitehealthy. They can eat without difficulty and seem to be influenced in a very early life. However, fluid that fills areas where brain hemispheres are often accumulated and can cause hydrocephalus. Other children may have seizures or twitching, they cannot be nursing or bottles, be blind or deaf and to some extent paralyzed.

It may be impossible to treat hydramentphalci. The missing brain cannot be replaced. However, there are treatment of different conditions with it. Some children receive bends to prevent or reduce the accumulation of fluids in the brain. Further treatment are administered on the basis of need, such as support for feeding, drugs to calm seizures and possibly professional or physical therapy.

One of the most respected aspects of hydramentphalia is trying to understand the summary of mortality and mortality. Most literature on this topic repeats that many children die before reaching the age of one. There is a highA percentage of children suffering from this unfortunate fate. On the other hand, there is also a fair percentage of children who live after the first year and can live in their adolescents or in the early 20 years.

Of course, children will require considerable support. A large amount of mental disability is expected and children may need special care after their lives. Parents also benefit from support, because being a long -term career of a sick child can sometimes be stressful and demanding. There are several Internet groups that provide support for parents and parents for those who raise children with hydramentphali. This can be quite useful in coping with very difficult aspects of this condition.