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There is no cystic fibrosis centre in Pakistan But Agha khan hospital karachi is best to diagnoseand treat cystic fibrosis patients .Almost all the medications of cystic fibrosis are available in Pakistan.

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Q: How many center in Pakistan on cystic fibrosis?
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Related questions

How long does cystic fibrosis last?

The person who has Cystic Fibrosis has it for life.


What disease is called by a genetic mutation?

cystic fibrosis


is cystic fibrosis affect the human body?

Cystic fibrosis is widely recognized as a lung disease, but it is actually a disease that affects many parts of the body. So yes. it can:) hope this is helpful


Does religion have an impact on cystic fibrosis?

Unfortunately, cystic fibrosis cannot be cured by prayer. If it could be cured by prayer, the disease would have disappeared a long time ago, because there are a great many people praying all the time. We have a great abundance of prayer, in this world. But we still have cystic fibrosis.


How many people have cystic fibrosis in Europe in the year 1985?

1 in every 8000


How many people die of cystic fibrosis a year?

go to www.cdc/gov.com :D hope i helped


How many people in the world have cf?

9,000 people (and counting) have cf (full name Cystic Fibrosis) hope this answer helped :-)


How many people died from cystic fibrosis in each year?

Deaths from Cystic Fibrosis: 485 deaths (NHLBI 1999)Death rate extrapolations for USA for Cystic Fibrosis: 484 per year, 40 per month, 9 per week, 1 per day, 0 per hour, 0 per minute, 0 per second. Note: this extrapolation calculation uses the deaths statistic: 485 deaths (NHLBI 1999)45 people died from cystic fibrosis in Australia 2000 (Australia's Health 2004, AIHW)Source(s):RRT


How many people have cystic fibrosis in the US?

Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). http://www.cff.org/


How many Caucasians in North America carry the unexpressed cystic fibrosis allele?

Forty-three of every 1,000. Hope this helps.


How many copies of an allele need to be present for someone to have cystic fibrosis?

Both cystic fibrosis and sickle cell anemia are single mutation diseases - one mutation in a single gene is enough to cause the disease. However, for cystic fibrosis both alleles of the gene must be mutated for the disease to develop. For sickle cell anemia, only one allele can carry the mutation and some signs of the disorder will be present. Having two alleles with the mutation causes much more significant disease.


What's Cystic fibrosis?

Cystic fibrosis is a genetic disorder which affects the lungs and pancreas. It causes the lungs to get clogged with mucus, which in turn makes the lungs a breeding ground for bacteria. In the pancreas, it blocks the pancreas from absorbing enzymes, which makes its victims prone to malnutrition. Often times, they have to take treatments such as lung therapy every day, as well as enzyme supplements on a daily basis. The average life expectancy is 37.Cystic Fibrosis is caused by a defective gene which causes a thick, sticky mucus. It builds up in the lungs and pancreas (the organ that helps to break-down food.) Cystic Fibrosis results in life-threatening lung infections and digestive problems. Symptoms are varied, but the most common are: No bowel movements in first 24 - 48 hours of life (baby!) Stools that are pale or clay colored, foul smelling or float. Infants can have salty tasting skin. Recurrent respiratory infections, such as pneumonia or sinusitis. Coughing/wheezing. Weight loss or can't gain weight normally in childhood. Diarrhea, delayed growth and fatigue.Cystic Fibrosis is the most common fatal genetic disease occurring in about 1 in 30,000 births. The gene must be inherited from both the mother and the father. Children inheriting only one copy of the gene are carriers but do not display symptoms. Average life expectancy for Cystic Fibrosis is approximately 32 years of age. There are many treatments but no cure. People with Cystic Fibrosis are at high risk of developing other conditions such as Cystic Fibrosis related Arthritis and Cystic Fibrosis related Diabetes, Liver failure and ultimately respiratory failure leading to death. Once a person with Cystic Fibrosis loses enough lung function the only other treatment is a lung transplant