Specific Genetic Mutation
The gene, called cystic fibrosis transmembrane conductance regulator, or CFTR, lies in the middle of chromosome 7 and encodes a protein of the same name, designated CFTR.
Physical Characteristics
Physical characteristics include chronic respiratory infections, chronic coughing, and shortness of breathe.
Possible Treatment
Treatments include the intake of pancreatic enzyme supplements and a diet high in calories, protein, and fat, physical therapy, medications, and bronchodilators.
Interesting Fact
Cystic fibrosis is an inherited disorder mainly affecting people of European ancestry.
"cystic fibrosis (CF)". Encyclopædia Britannica. Encyclopædia Britannica Online.
Encyclopædia Britannica Inc., 2015. Web. 04 Nov. 2015
<http://www.britannica.com/science/cystic-fibrosis>.
https://www.snowballeffect.co.nz
Encyclopædia Britannica Inc., 2015. Web. 04 Nov. 2015
<http://www.britannica.com/science/cystic-fibrosis>.
https://www.snowballeffect.co.nz