MRCP UK EXAMINATIONS

Detailed explanation-1: -Currently there’s no cure for rare types of cystic fibrosis, but researchers are making significant advances. Current treatments for cystic fibrosis are not suitable for all patients. The lack of treatment options is distressing for people suffering from a rare type of this degenerative and life-threatening disease.

Detailed explanation-2: -Many young adults with CF finish college or find jobs. Lung disease eventually worsens to the point where the person is disabled. Today, the average life span for people with CF who live to adulthood is about 44 years. Death is most often caused by lung complications.

Detailed explanation-3: -Mucus in CF patients is very thick and accumulates in the intestines and lungs. The result is malnutrition, poor growth, frequent respiratory infections, breathing difficulties, and eventually permanent lung damage.

Detailed explanation-4: -Studies using CRISPR gene editing tools will correct genes in the cells that line the airways. Using these tools could lead to new treatments for genetic and acquired lung disease. A research program is developing combinatorial non-viral and viral CRISPR delivery for lung diseases.