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The term childhood disease refers to disease that is contracted or becomes symptomatic before the age of 18 or 21 years old. Many of these diseases can also be contracted by adults. Some childhood diseases include:
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child.
Chronic diseases in children may have a genetic (hereditary) cause, an environmental (acquired) cause or a combination of both. Early identification and treatment of the disease is key to successful health outcomes. Chronic diseases can affect multiple organ systems and can, therefore, manifest in different ways.
Rare disease This page was last edited on 28 September 2024, at 13:01 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...
The opposite of a hereditary disease is an acquired disease. Most cancers , although they involve genetic mutations to a small proportion of cells in the body, are acquired diseases. Some cancer syndromes , however, such as BRCA mutations , are hereditary genetic disorders.
One 2022 study found that the risk of Peyronie’s disease was significantly higher in the immediate family members of men with the disease, including parents, siblings, and children. But don’t ...
Kawasaki disease (also known as mucocutaneous lymph node syndrome) is a syndrome of unknown cause that results in a fever and mainly affects children under 5 years of age. [6] It is a form of vasculitis, where medium-sized blood vessels become inflamed throughout the body. [1]
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