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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. There are over 6,000 known genetic disorders in humans.
Heart disorders (Congenital heart defects) ... Rare disease This page was last edited on 28 September 2024, at 13:01 (UTC). Text is available under the Creative ...
According to the Boston Children’s Hospital, approximately 14,000 children in the world have been diagnosed with the disease. Specifically in the U.S., it’s estimated that “2 to 4 out of ...
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A rare disease is technically defined ... Behçet's disease; Benign acute childhood myositis; ... List of disorders included in newborn screening programs;
Childhood dementia is an umbrella group of rare, mostly untreatable neurodegenerative disorders that show symptoms before the age of 18. These conditions cause progressive deterioration of the brain and the loss of previously acquired skills such as talking, walking, and playing.
Many rare diseases appear early in life, and about 30% of children with rare diseases will die before reaching their fifth birthdays. [1] Fields condition is considered the rarest known disease, affecting three known individuals, two of whom are identical twins. [ 2 ]