0
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.
Wiki User
∙ 9y ago
Wiki User
∙ 13y agorecessive genes!
Add your answer:
Earn +20 pts
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 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 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 is the medical term meaning liver inflammation and fibrosis?
Cirrhosis is defined as liver inflammation and fibrosis. Liver inflammation is hepatitis. Fibrosis is fibrosis.
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 pumilary fibrosis?
Pulmonary fibrosis is another term for scarring in the lungs. It is often caused by infections, smoking, or exposure to asbestos.
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.
What is the term for biological inheritance?
heredity
What is the medical term meaning cystic tumor that develops on a tendon?
ganglioma
