Rare diseases and Orphan drugs

A Rare disease is any illness affecting a significantly smaller percentage of the population. Most genetic disorders are inherited, and thus persist throughout the individual's entire life and are caused directly by gene or chromosome changes. For certain cases genetic shifts are transmitted from generation to generation. In other cases, they occur at random in a person who is the first to be diagnosed in a family. Lots of unusual illnesses occur early in life. The exact cause for many rare diseases remains unknown. But Environmental factors, viral infections, genetic mutations, diet, smoking, or exposure to chemicals, also can play a role in rare diseases. Many rare diseases, including infections, a few rare cancers, and a few immune system infections, are not inherited. While researchers are learning more each year, the correct cause of many rare diseases is still unknown. Researches are still going on for this uncommon illness.

    Related Conference of Rare diseases and Orphan drugs

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