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The term that best describes the inheritance of cystic fibrosis is that it is genetic. Cystic fibrosis is caused by recessive alleles. Cystic fibrosis is an autosomal recessive genetic disease.
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What term describes the inheritence cystic fibrosis?
The term that best describes the inheritance of cystic fibrosis is that it is genetic. Cystic fibrosis is caused by recessive alleles. Cystic fibrosis is an autosomal recessive genetic disease.
What term inheritance of cystic fibrosis?
recessive genes!
What is the term for Cystic fibrosis?
Hardening of the outer wall of the cell
Medical term that begins with n?
a nebulizer is an item that is used for some cystic fibrosis paitece.
What is the Salty Baby disorder?
Perhaps cystic fibrosis?Cystic Fibrosis-- Final answer. CFTR channels malfunction and Chloride cannot exchange with bicarb at the epithelial surfaces exposed to the environment. Chloride then gets stuck outside the environment.
What are cystic fibers?
If you're talking about "fibrocystic" breasts, it means that there are small cysts in the breast tissue that react to things like how much caffeine (makes them worse) or how much fiber (makes them not as bad) you take in. If you're talking about "cystic fibrosis," that is something different.
What is the long term prognosis for a cystic fibrosis sufferer?
The long-term prognosis for someone with cystic fibrosis varies greatly from person to person. Genetic mutations, modifier genes, environmental factors, and, to some degree, luck can all influence the progression of the disease. Many people with cystic fibrosis live into their 20s, 30s, and beyond but there are some that do not. There are exciting new drug therapies in the pipeline that have the ability to change cystic fibrosis from a life-shortening disease to a completely manageable disease. For instance, the drug Kalydeco is considered a functional cure for a certain subset of the CF population.
What condition causes the airways to become inflamed and thickened and an increase in the number and size of mucus producing cells?
Chronic bronchitis is a condition that causes inflammation and thickening of the airways, leading to excess mucus production. This can result in symptoms such as cough, shortness of breath, and recurrent respiratory infections. It is often associated with smoking and long-term exposure to irritants.
What term describes the inheritance of cysticfibrosis?
Cystic fibrosis is an autosomal recessive disease. That means that each parent has to carry a mutation and will have a 1 in 4 (25%) chance of having a child with CF. The previous answer is not correct. __________________________________________________________________ You inherit cystic fibrosis from either one parent or both. It is to do with genetic mapping. Cystic fibrosis is a recessive gene and can be carried by our parents even if they do not suffer from it, it's like in a carrier(someone who does not suffer from CF but still has the gene) the cystic fibrosis gene is 'hiding'. When we crete gametes (sperm and eggs) the genes have to split. For example your father could have the gene Ff and they would split and become F f. The capital F is the dominant gene and the small f is the recessive gene, in this case cystic fibrosis. When an egg is fertilised the separate gene from both parents join together. If a man and women have one child, and both parents had the recessive gene of CF then the likelihood of their first child having cystic fibrosis is high, 50% in fact. Here is a diagram which might help explain Parents Mother + Father Genotype (genes) Ff Ff Gametes(sperm+egg) F f F f Offspring FF ff 50% 50% I hope this helped a little. I didn't go into full detail becasue there is a lot more to it then what i have said and it is a lot more comlicated. If you can, try to go on a revision site which may help.
What complications are associated with ABPA?
Patients with ABPA sometimes cough up large amounts of blood, a condition that is called hemoptysis. They may also develop a serious long-term form of bronchiectasis.ABPA sometimes occurs as a complication of cystic fibrosis.
What is the medical term meaning liver inflammation and fibrosis?
The medical term for liver inflammation and fibrosis is "hepatitis." This condition can lead to scarring of the liver, known as fibrosis, and if left untreated, can progress to cirrhosis, where the liver becomes severely scarred and may eventually fail.
How does cystic fibrosis affects the body?
Cystic Fibrosis is a chronic, long term life-threatening condition effects the lungs, digestive system, pancreas, and sometimes the liver and sex organs. It is a inherited disorder, and can only be passed down from two parents who are cf carriers, meaning a defective CFTR gene. About 10 million Americans are symptomless carriers of cystic fibrosis. People with cf produce an abnormal amount of thick, sticky mucous that clog the lungs and ducts in the pancreas, leading to chronic lung infections, coughing and difficulty breathing. It also obstructs the ducts in the pancreas, which blocks the enzymes from entering the intestines leading malabsorption. Children with cystic fibrosis have a hard time gaining weight and growing normally; the have to consume more calories than their peers to keep their weight at an average for how tall they are. The symptoms of cystic fibrosis vary from person to person. They may include -salty skin -shortness of breath/wheezing -Bulky, greasy stools -weight loss -frequent infections; pneumonia, bronchitis etc., -nasal polyps -abdominal bloating/gas There is no cure for cystic fibrosis, but patients can control their symptom by medications, (antibiotics, inhalers, enzymes, and sometimes a feeding tube if not able to gain weight), airway clearance, and proper nutrition. Eventually lung damage may become so severe that a lung transplant is needed. In 1985, the average life expectancy was 25. Thanks to research and updated medical care, the life expectancy in 2007 was 37.4, which continues to increase.
