Cystic Fibrosis Statistics

Cystic Fibrosis is a disease caused by genetic abnormality of the CFTR gene. This results in modified secretions throughout the body. These secretions are normally produced by the body serving a variety of vital functions. When the secretions are abnormal, many of these functions are compromised.

This is a serious disease and affects many people. The following are just some of the statistics of this condition.

• Approximately 805 of children diagnosed with Cystic Fibrosis have parents that do not exhibit any symptoms. This is because Cystic Fibrosis is inherited as a recessive genetic disease.
• Of the children diagnosed, this usually happens between the ages of 3 months old and 6 years.
• Over 50% of Cystic Fibrosis patients are hospitalized at least once a year for approximately 10 days.
• Cystic Fibrosis affects Caucasians the most (1:3,300) followed by Hispancis (1:9,500). Non-caucasian populations are affected far less (1:12,000).
• In the United States, the median age of survival in 2005 was approximately 37 years, up from 33 years in 2002.
• More than ten million people in the United States are carriers of the mutated gene and do no know this.
• There is approximately a 72% one-year survival rate for living lung donor transplantation rate.
• There are about one thousand new cases of Cystic Fibrosis diagnoses every year.

Cystic Fibrosis Statistics

These are just limited statistics but they paint a very clear picture of the seriousness of this disease. Research is on-going and is making progress as illustrated by the median age of survival. However, more research must be done to totally eliminate this disease.