What is some history of cystic fibrosis?

What is some history of cystic fibrosis?

The first modern description of the disease was made in 1938 by pathologist Dorothy Andersen. Based on autopsies of children who had died of malnutrition, she termed the disease “cystic fibrosis of the pancreas.” It had previously been known as “mucoviscidosis,” referring to the thickening of mucus.

What chromosome is cystic fibrosis on?

Cystic fibrosis is a disease that is caused by an abnormal gene. An abnormal gene is called a genetic mutation. The gene that causes problems in CF is found on the seventh chromosome. There are many mutations (abnormal genes) that have been shown to cause CF disease.

Who was the first person to find out cystic fibrosis?

In 1938, American pathologist Dr. Dorothy Andersen provided the first description of the disorder in the medical literature, calling the disease “cystic fibrosis of the pancreas” based on her autopsy findings of children who died of malnutrition.

What is life expectancy with CF?

In some cases, CF can be a mild disease. But in most people with CF, it poses a serious risk to a person’s health. The average lifespan of a person with CF is 37 years. Those with a milder form can live into their 50s.

Why does cystic fibrosis shorten the lifespan?

Cystic fibrosis is a genetic disease, and it has no cure. Medications can improve symptoms, but the disease can’t be eradicated. This disorder shortens lifespan because it affects lungs, pancreas along with various complications in the body.

What is the death rate of cystic fibrosis?

Death Rate Extrapolation. Death rate extrapolations for USA for Cystic Fibrosis: 484 per year, 40 per month, 9 per week, 1 per day, 0 per hour, 0 per minute, 0 per second.

In 1938, American pathologist Dr. Dorothy Andersen provided the first description of the disorder in the medical literature, calling the disease “cystic fibrosis of the pancreas” based on her autopsy findings of children who died of malnutrition.

In some cases, CF can be a mild disease. But in most people with CF, it poses a serious risk to a person’s health. The average lifespan of a person with CF is 37 years. Those with a milder form can live into their 50s.

Cystic fibrosis is a genetic disease, and it has no cure. Medications can improve symptoms, but the disease can’t be eradicated. This disorder shortens lifespan because it affects lungs, pancreas along with various complications in the body.

Death Rate Extrapolation. Death rate extrapolations for USA for Cystic Fibrosis: 484 per year, 40 per month, 9 per week, 1 per day, 0 per hour, 0 per minute, 0 per second.