rare_disease

A rare disease is any disease that affects a small percentage of the population. In some parts of the world, an orphan disease is a rare disease whose rarity means there's a lack of a market large enough to gain support and resources for discovering treatments for it, except by the government granting economically advantageous conditions to creating and selling such treatments. Orphan drugs are ones so created or sold.

Most rare diseases are genetic and thus are present throughout the person's entire life, even if symptoms do not immediately appear. Many rare diseases appear early in life, and about 30% of children with rare diseases will die before reaching their fifth birthday.

With a single diagnosed patient only, ribose-5-phosphate isomerase deficiency is considered the rarest known genetic disease.

No single cutoff number has been agreed upon for which a disease is considered rare. A disease may be considered rare in one part of the world, or in a particular group of people, but still be common in another.

American organisation Global Genes have estimated that more than 300 million people worldwide are living with one of the 7,000 diseases they define as “rare” in the United States.

  • rare_disease.txt
  • Last modified: 2018/05/10 11:34
  • by administrador