Presentation is loading. Please wait.

Presentation is loading. Please wait.

Cystic Fibrosis.

Similar presentations


Presentation on theme: "Cystic Fibrosis."— Presentation transcript:

1 Cystic Fibrosis

2 What is cystic fibrosis
Cystic fibrosis is an inherited disease that causes thick, sticky mucus to build up in the lungs and digestive tract. It is one of the most common chronic lung diseases in children and young adults, and may result in early death.

3 Symptoms Symptoms in newborns may include: Delayed growth
Failure to gain weight normally during childhood No bowel movements in first 24 to 48 hours of life Salty-tasting skin Symptoms related to bowel function may include: Belly pain from severe constipation Increased gas, bloating, or a belly that appears swollen (distended) Nausea and loss of appetite foul smelling, have mucus, or that float Weight loss Symptoms related to the lungs and sinuses may include: Coughing or increased mucus in the sinuses or lungs fatigue Nasal congestion caused by nasal polyps Recurrent episodes of pneumonia. Symptoms in someone with cystic fibrosis include: Fever Increased coughing Increased shortness of breath Loss of appetite More sputum

4 Cause of Cystic Fibrosis
CF cannot be "caught" like a cold or the flu. It's genetic and is caused by inheriting two copies of the same abnormal gene, one from each parent. People who get one defective and one normal copy of the gene are said to be "carriers" of the CF gene. Carriers don't get CF, but they have the abnormal CF gene that can be passed on to their children. Relative with CF Your carrier risk Parent or child 1 in 1 (100%) Siblings 2 in 3 (67%) Niece or nephew 1 in 2 (50%) Aunt or uncle 1 in 3 (33%) Cousin 1 in 4 (25%)

5 Hereditary disease The disease is passed from parents to children through genes. People who have cystic fibrosis inherit two faulty genes for the disease—one from each parent. The parents likely don't have the disease themselves.

6 Treatments for cystic fibrosis
Treatment includes digestive enzyme supplements, dietary changes, immunizations, physical therapy, and medications. More recently, some CF patients with terminal lung disease have received lung transplants. Children need to eat a well-balanced diet rich in calories and protein. Keeping a child's immunizations (vaccine shots) up to date is extremely important to protect them from infections.


Download ppt "Cystic Fibrosis."

Similar presentations


Ads by Google