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Published byChad Bryan Modified over 8 years ago
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By: Paige Whalen and Alex Ung
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Mutation in the gene called cystic fibrosis transmembrane conductance regulator. Due to loss of chromosome, located on chromosome 7. Recessive
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Symptoms occur throughout the whole body Newborns: Delayed growth Bowels: Severe constipation Lungs: Mucus build up
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Blood tests look for variations of the gene in CFTR. Exercising Medicines (antibiotics, anti-inflammatory, bronchodilators) Lung transplants for critical conditions
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Cystic Fibrosis is common in the Caucasian population in the US. 1 in 2,500-3,500 Caucasian newborns 1 in 17,000 African Americans 1 in 31,000 Asian Americans
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Using artificial insemination can help many out by preventing financial issues, also loosing a family member. Testing should be done, if you treat the disease it can prevent lung infections and breathing problems. Lowering the chance of a kid having the disease would help since the disease can cause pain and death. Question 5
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Most people are detected with CF during a newborn screening. Diagnosing the disease is easily done with blood tests.
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