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As of recent estimates, there are about 10,000 people living with cystic fibrosis (CF) in the UK. The condition is one of the most common genetic disorders in the country, affecting individuals of all ages. Advances in treatment have improved life expectancy and quality of life for many patients.
What else can I help you with?
What are the main advantages of CF cards?
There are many advantages of CF cards. The main advantage is that CF cards are able to store more data. They offer more reliable storage and can be used in Bluetooth, Wi-Fi and digital cameras.
When was Mora CF created?
Mora CF was created in 1977.
When was Muleño CF created?
Muleño CF was created in 1989.
When was Andorra CF created?
Andorra CF was created in 1957.
When was Huracán CF created?
Huracán CF was created in 2011.
When was Cayston a drug used to treat lung infections caused by Cystic Fibrosis first invented?
Cayston or Azli is quite a new drug and in the UK it has recently (last year or so) been offered to those suffering with the Pseudomonas aeruginosa bug that the majority of CF sufferers have.
What is a closed angle glaucoma?
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What do the letters CF after someone's name mean?
It may "Chaplain of the Forces" for a UK Armed Forces Chaplain.
How many Down syndrome sufferers in Australia?
Just the 1
How many people are affected with CF?
CF affects approximately 30,000 children and young adults in the United States, and about 3,000 babies are born with CF every year.
How many people had cf in 1970?
43000
How many people had cf in 2005?
83000
How many 60 lb bags of concrete in a half yard?
1 CY = 27 CF. One half yard = 13.5 CF. 13.5 CF /.45 CF per 60 Lb. bag = 30 Bags
How many gallon of water are in a cf?
7.48 gallons
What is the purpose of a CF memory card?
There are many purposes of a CF memory card. CF memory cards can be used for mass storage purposes. They are also used for camcorders and high definition cameras.
What is the risk in each pregnancy of having a child with cystic fibrosis?
By "another pregnancy", I assume that the parents have had one child with cystic fibrosis. As cystic fibrosis is recessive and neither parent suffers from it, they must both be carriers. That means the chances of the next baby having CF is 25%, or a one in four chance. Assuming both parents have one CF and one non-CF gene, the combinations work out: non-CF x non-CF (normal) non-CF x CF (carrier) CF x non-CF (carrier) CF x CF (cystic fibrosis sufferer) Therefore their chances of having a: normal child = 25% child who is a CF carrier = 50% child who suffers from CF = 25%
Why is protein bad for gout sufferers?
There are many purine rich proteins that should be avoided by gout sufferers as purines turn into uric acid which in turn turn into crystals that cause gout.
