Is cystic fibrosis due to chromosome damage?

Is cystic fibrosis more common in boys or girls?

i copied the following answer from health.howstuffworks.com Unlike some other genetic conditions, cystic fibrosisoccurs equally as often in men and women. The genetic mutation for cystic fibrosis occurs on chromosome 7 and is not impacted by gender. The severity of symptoms related to cystic fibrosis, however, does vary in men and women. In particular, girls with cystic fibrosis have more difficulty with meeting growth milestones and experience more lung-related problems compared to boys. Due to these more severe symptoms, women with cystic fibrosis have shorter life expectancies than men. It is estimated that men with cystic fibrosis live four to five years longer than women with cystic fibrosis, Moreover, under the age of 20, girls have a 60 percent greater chance of dying due to cystic fibrosis complications compared to males [source: Cystic Fibrosis Worldwide]. As a result, the prevalence of male adults with cystic fibrosis is greater than the prevalence of female adults with cystic fibrosis, suggesting a male advantage with the disorder. Cystic fibrosis researchers argue that this gender difference is the result of early-onset lung infections in girls. Girls appear to develop these infections earlier in life than boys, leading to more severe cystic fibrosis complications, and even death. Girls also appear to have greater difficulty maintaining a healthy body weight after puberty compared to males, which places girls at greater risk for cystic fibrosis complications. It appears that this gender gap can narrow if girls are provided with more intensive medical care. In fact, girls and women who receive regular intravenous antibiotics, regardless of their condition, have improved survival rates [source: Cystic Fibrosis Worldwide]. As a result, countries with excellent health care, such as Scandinavian countries, do not have a difference in the survival rate of men and women with cystic fibrosis. i hope it helps:)

How does cystic fibrosis affect homeostasis?

Cystic fibrosis happens due to mutations in a gene called CFTR and an abnormal behavior impairs homeostasis inside the cell. Cyst

What can rectal prolapse be a sign of in children?

In children it is often an early sign of cystic fibrosis or is due to neurological or anatomical abnormalities.

How does cystic fibrosis affect the urinary system?

Cystic fibrosis primarily affects the respiratory and digestive systems, but it can also have implications for the urinary system. The thick mucus characteristic of the disease can lead to complications in the kidneys, such as kidney stones or urinary tract infections, due to dehydration and imbalances in salt and fluid levels. Additionally, cystic fibrosis can result in reduced kidney function over time, complicating the body's ability to regulate electrolytes and maintain fluid balance. However, the urinary system is generally less affected than other systems in cystic fibrosis.

Why do inherited diseases like hemophilia and cystic fibrosis occur?

They are caused by the genes that we inherit from our parents. Genes govern how our body is run. Cystic fibrosis is caused by a recessive alle. This means that both parents must be carriers of the alle responsible for cystic fibrosis. The parents don't have to have the condition themselves; they can be just carriers of the one alle that makes up the condition.

Why are Filipinos not affected by cystic fibrosis?

The lower prevalence of cystic fibrosis in Filipinos is believed to be due to genetic factors. Filipinos may have a different genetic makeup that reduces their risk of developing this condition compared to other populations. Additionally, environmental factors may also play a role in the low incidence of cystic fibrosis in Filipinos.

Do people with Cystic Fibrosis die young?

The life expectancy of individuals with cystic fibrosis has significantly improved over the years due to advancements in treatments and therapies. However, it is still considered a life-shortening disease, with most individuals living into their 30s and 40s. With proper management and care, many people with cystic fibrosis can lead fulfilling lives.

What disease is most common for white people?

Skin cancer, particularly melanoma, is most common among white people. This is due to the decreased melanin in their skin, which provides less protection against UV radiation. Regular sun protection and skin checks are recommended for prevention and early detection.

What disease does cystic fibrosis protect you from?

Cystic fibrosis (CF) provides a protective effect against certain forms of tuberculosis, particularly due to the mutation in the CFTR gene that affects ion transport in cells. This mutation leads to changes in the environment of the lungs and airways, which can inhibit the growth of Mycobacterium tuberculosis. Additionally, the thick mucus associated with CF can create a hostile environment for some pathogens, including those that cause respiratory infections. However, it's important to note that cystic fibrosis comes with significant health challenges and is primarily considered a serious genetic disorder.

What glands does cystic fibrosis affect?

Cystic fibrosis primarily affects the exocrine glands, particularly the lungs, pancreas, sweat glands, and digestive system. In the lungs, it leads to thick mucus buildup, causing respiratory issues. The pancreas is affected by obstructed ducts, impairing digestion and nutrient absorption. Additionally, sweat glands produce saltier sweat due to altered electrolyte transport.

Does the Cystic Fibrosis Foundation support embryonic stem cell research?

"The Cystic Fibrosis Foundation is not involved in funding research on the use of human embryonic stem cells. The CF Foundation has provided funds to an institution for research on human adult stem cells for CF research. This research grant is approximately $40,000 in total."American Journal of Respiratory and Critical Care Medicine Vol 173. pp. 1043-1045, (2006)http://ajrccm.atsjournals.org/cgi/content/full/173/9/1043

How do you die from cystic fybrosis?

People with cystic fibrosis often die from respiratory failure due to the thick, sticky mucus that clogs their lungs. This leads to chronic lung infections and progressive lung damage, ultimately making it difficult to breathe and leading to respiratory failure. In some cases, complications from these chronic infections or other organ involvement can also contribute to the fatal outcome.