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 Types
amniocentesis
- This test, performed upon a sample of the fluid surrounding the foetus in the uterus (the "amniotic fluid"), is designed to detect a number of disorders of the foetus.
Autism
Autism - One in a thousand children are born with autism, a condition for which there's no cure and no medical treatment. But it can be managed. Peta Newbold reports: - When seven-year old twins Corey and Harley Williams returned home...
cystic fibrosis - nutritional considerations
- Cystic fibrosis (CF) is a genetic disease. CF occurs in 1 in 2500 births in Australia and is the most common genetic disease in Caucasian Australians. CF prevents the body from absorbing enough nutrients. This makes it difficult for people with CF to meet increased nutrient needs. As a result, people with CF may need to eat an enriched diet with more kilojoules and take extra vitamins and enzymes.
epilepsy
genetic screening
- Genetic screening is the process of looking for indications of a genetic disease. A genetic disease is a condition that is passed down from a parent to his or her offspring. Genetic screening is usually done before any signs of disease are present. The procedure is undertaken for several reasons. It may be done to determine if someone will develop a genetic disease. Examples of common genetic disorders are: Turner syndrome Down syndrome Klinefelter syndrome Tourette syndrome coeliac disease Wilson disease Huntington disease Duchenne muscular dystrophy Tay-Sachs disease haemachromatosis cystic fibrosis thallasaemiaGenetic screening is sometimes done to determine if a person can pass on a genetic disease, even if he or she is not at risk for developing the actual condition. It also may be done as part of a study of the whole population.
genetic testing
- Through genetic testing, doctors look for the known cause of a specific disease in someone who already has the symptoms. Laboratory studies can determine whether someone has a genetic disease. Genetic screening, on the other hand, is a more general search for inherited problems, to see if any exist. Genes are inherited building blocks that determine a person's physical traits such as height or eye colour. A defect in a gene can cause inherited diseases.
hemiplegia
hydrocephalus in children
- Hydrocephalus is a condition involving the abnormal accumulation of cerebrospinal fluid in and around the brain.
phenylketonuria
dyslexia
speech disorders in children
Tay-Sachs disease
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