Crossword Solver > found answer > CYSTICFIBROSIS (cystic fibrosis)

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cysticfibrosis

cystic fibrosis

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The answer CYSTICFIBROSIS (cystic fibrosis) has 0 possible clue(s) in existing crosswords.

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The word CYSTICFIBROSIS (cystic fibrosis) is NOT valid in any word game. (Sorry, you cannot play CYSTICFIBROSIS (cystic fibrosis) in Scrabble, Words With Friends etc)

There are 14 letters in CYSTICFIBROSIS ( B³C³F⁴I¹O¹R¹S¹T¹Y⁴ )

To search all scrabble anagrams of CYSTICFIBROSIS, to go: CYSTICFIBROSIS?

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3 letters out of CYSTICFIBROSIS

BIO BIS BIT BOS BOT BOY BRO BYS CIS COB COR COS COT COY CRY FIB FIR FIT FOB FOR FOY FRO FRY ICY IFS ITS OBI OFT ORB ORC ORS ORT RIB RIF ROB ROC ROT SIB SIC SIR SIS SIT SOB SOS SOT SOY SRI STY TIC TIS TOR TOY TRY YOB

2 letters out of CYSTICFIBROSIS

BI BO BY IF IS IT OF OI OR OS OY SI SO TI TO YO

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Definitions of cystic fibrosis in various dictionaries:

noun - the most common congenital disease

CYSTIC FIBROSIS - the most common congenital disease; the child's lungs and intestines and pancreas become clogged with thick mucus; caused by defect in a single gene; no cure is known

CYSTIC FIBROSIS - Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine. Long-term issues incl...

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Possible Jeopardy Clues
Dorothy Hansine Andersen identified this disease abbreviated CF & devised a test to diagnose it
CFTR, the defective gene responsible for transmitting this metabolic disease, lies in the middle of chromosome 7
Great Strides is a fundraising event used in "taking steps to cure" this disease, CF for short
In 1989 researchers identified the abnormal gene on chromosome 7 that causes CF, this disease
(Dr. Oz presents the clue.) Dr. Dorothy Andersen named this disease, CF for short, & also helped create a test to diagnose it

Cystic fibrosis description
Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine. Long-term issues include difficulty breathing and coughing up mucus as a result of frequent lung infections. Other signs and symptoms may include sinus infections, poor growth, fatty stool, clubbing of the fingers and toes, and infertility in most males. Different people may have different degrees of symptoms.CF is inherited in an autosomal recessive manner. It is caused by the presence of mutations in both copies of the gene for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. Those with a single working copy are carriers and otherwise mostly normal. CFTR is involved in production of sweat, digestive fluids, and mucus. When the CFTR is not functional, secretions which are usually thin instead become thick. The condition is diagnosed by a sweat test and genetic testing. Screening of infants at birth takes place in some areas of the world.There is no known cure for cystic fibrosis. Lung infections are treated with antibiotics which may be given intravenously, inhaled, or by mouth. Sometimes, the antibiotic azithromycin is used long term. Inhaled hypertonic saline and salbutamol may also be useful. Lung transplantation may be an option if lung function continues to worsen. Pancreatic enzyme replacement and fat-soluble vitamin supplementation are important, especially in the young. Airway clearance techniques such as chest physiotherapy have some short-term benefit, but long-term effects are unclear. The average life expectancy is between 42 and 50 years in the developed world. Lung problems are responsible for death in 80% of people with cystic fibrosis.CF is most common among people of Northern European ancestry and affects about one out of every 3,000 newborns. About one in 25 people is a carrier. It is least common in Africans and Asians. It was first recognized as a specific disease by Dorothy Andersen in 1938, with descriptions that fit the condition occurring at least as far back as 1595. The name "cystic fibrosis" refers to the characteristic fibrosis and cysts that form within the pancreas.

Cystic fibrosis description

Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine. Long-term issues include difficulty breathing and coughing up mucus as a result of frequent lung infections. Other signs and symptoms may include sinus infections, poor growth, fatty stool, clubbing of the fingers and toes, and infertility in most males. Different people may have different degrees of symptoms.CF is inherited in an autosomal recessive manner. It is caused by the presence of mutations in both copies of the gene for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. Those with a single working copy are carriers and otherwise mostly normal. CFTR is involved in production of sweat, digestive fluids, and mucus. When the CFTR is not functional, secretions which are usually thin instead become thick. The condition is diagnosed by a sweat test and genetic testing. Screening of infants at birth takes place in some areas of the world.There is no known cure for cystic fibrosis. Lung infections are treated with antibiotics which may be given intravenously, inhaled, or by mouth. Sometimes, the antibiotic azithromycin is used long term. Inhaled hypertonic saline and salbutamol may also be useful. Lung transplantation may be an option if lung function continues to worsen. Pancreatic enzyme replacement and fat-soluble vitamin supplementation are important, especially in the young. Airway clearance techniques such as chest physiotherapy have some short-term benefit, but long-term effects are unclear. The average life expectancy is between 42 and 50 years in the developed world. Lung problems are responsible for death in 80% of people with cystic fibrosis.CF is most common among people of Northern European ancestry and affects about one out of every 3,000 newborns. About one in 25 people is a carrier. It is least common in Africans and Asians. It was first recognized as a specific disease by Dorothy Andersen in 1938, with descriptions that fit the condition occurring at least as far back as 1595. The name "cystic fibrosis" refers to the characteristic fibrosis and cysts that form within the pancreas.

Anagrammer Crossword Solver is a powerful crossword puzzle resource site. We maintain millions of regularly updated crossword solutions, clues and answers of almost every popular crossword puzzle and word game out there. We encourage you to bookmark our puzzle solver as well as the other word solvers throughout our site. Explore deeper into our site and you will find many educational tools, flash cards and plenty more resources that will make you a much better player. This page shows you that Dorothy Hansine Andersen identified this disease abbreviated CF & devised a test to diagnose it is a possible clue for cystic fibrosis. Cystic fibrosis: Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liv...