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Respond
to your colleagues and respectfully agree or disagree with your
colleague’s assessment and explain your reasoning. In your
explanation, include why their explanations make physiological
sense or why they do not
At least 2 references in each peer responses!
Cystic Fibrosis is an autosomal recessive disease that affects
chromosome 7 on the DNA helix. The parents of the child with
cystic fibrosis are both carriers of the disorder and likely have
no symptoms and have no idea they are carriers. The disease is
caused by a mutation in cystic fibrosis transmembrane regulator
(CFTR). The CFTR regulates the flow of salt and fluids in and
out of the cell. The CFTR protein provides instructions for the
channel than transports negatively charged particles called
chloride ions in and out of the cell and across the tissues. The
lack of this channel causes the build-up of thick and sticky
mucus because chloride helps with the movement of water
across the tissues that assist with thinning the mucus. (CF
Genetics: The Basics, 2020)
The organs that are affected most frequently are the lungs,
digestive organs, pancreas, and reproductive organs. The thick
mucus causes frequent lung infections and the cyst in the lungs.
The thick mucus blocks the ducts of the pancreas and prevents
the transport of digestive enzymes leading to malnutrition. The
production of insulin is also affected by the thick mucus and
cystic fibrosis patients can develop diabetes-related to this.
Males with cystic fibrosis are infertile due to mucus plugging
the vas deferens. Female with cystic fibrosis frequently have
difficulty during pregnancy (Cystic Fibrosis, 2020).
Cystic fibrosis is a recessive disease and both parents must be
carries to produce a child who has cystic fibrosis. The chances
of two carriers having a child with cystic fibrosis are 25% and
the chances that the child will have a 50% chance they are a
carrier of the mutation and a 25% chance that the child will not
be a carrier or have the disease. The person with cystic
fibrosis has a child with a cystic fibrosis carrier then they have
a 50% chance the child will have cystic fibrosis and a 50%
chance they will be a carrier (Cystic Fibrosis, n.d.).
Cystic fibrosis is common in the Caucasian population with a
frequency rate of 1 in 2500-3500 births. African American have
a frequency rate of 1-17000 and Asian population have a
frequency rate of 1-3100 births (CF Genetics: The Basics, 2020)

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Respond to your colleagues and respectfully agree or disagree with.docx

  • 1. Respond to your colleagues and respectfully agree or disagree with your colleague’s assessment and explain your reasoning. In your explanation, include why their explanations make physiological sense or why they do not At least 2 references in each peer responses! Cystic Fibrosis is an autosomal recessive disease that affects chromosome 7 on the DNA helix. The parents of the child with cystic fibrosis are both carriers of the disorder and likely have no symptoms and have no idea they are carriers. The disease is caused by a mutation in cystic fibrosis transmembrane regulator (CFTR). The CFTR regulates the flow of salt and fluids in and out of the cell. The CFTR protein provides instructions for the channel than transports negatively charged particles called chloride ions in and out of the cell and across the tissues. The lack of this channel causes the build-up of thick and sticky mucus because chloride helps with the movement of water across the tissues that assist with thinning the mucus. (CF Genetics: The Basics, 2020) The organs that are affected most frequently are the lungs, digestive organs, pancreas, and reproductive organs. The thick mucus causes frequent lung infections and the cyst in the lungs. The thick mucus blocks the ducts of the pancreas and prevents the transport of digestive enzymes leading to malnutrition. The production of insulin is also affected by the thick mucus and cystic fibrosis patients can develop diabetes-related to this. Males with cystic fibrosis are infertile due to mucus plugging the vas deferens. Female with cystic fibrosis frequently have difficulty during pregnancy (Cystic Fibrosis, 2020).
  • 2. Cystic fibrosis is a recessive disease and both parents must be carries to produce a child who has cystic fibrosis. The chances of two carriers having a child with cystic fibrosis are 25% and the chances that the child will have a 50% chance they are a carrier of the mutation and a 25% chance that the child will not be a carrier or have the disease. The person with cystic fibrosis has a child with a cystic fibrosis carrier then they have a 50% chance the child will have cystic fibrosis and a 50% chance they will be a carrier (Cystic Fibrosis, n.d.). Cystic fibrosis is common in the Caucasian population with a frequency rate of 1 in 2500-3500 births. African American have a frequency rate of 1-17000 and Asian population have a frequency rate of 1-3100 births (CF Genetics: The Basics, 2020)