What organelle produces excess mucus in cystic fibrosis?

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 was the cause for Frederic Chopin's Death?

Frederic Chopin (1810-1849) died of tuberculosisbut in the eyes of the Polish cystic-fibrosisspecialist Wojciech Cichy, it is said that he died of cystic fibrosis, a genetic-disorderwhich clogs the lungwith excess thick, sticky mucus.

What is a recessive genetic disorder that affects chloride ion uptake in cells resulting in an osmotic imbalance recognized by excess mucus production?

Cystic fibrosis is a recessive genetic disorder that affects chloride ion uptake in cells, leading to an osmotic imbalance and excess mucus production in various organs, particularly affecting the lungs and digestive system. This can lead to breathing difficulties, frequent lung infections, and problems with digestion and nutrient absorption.

Which Genetic disorder is more common in Caucasians?

Hemochromatosis type 1 (or simply Haemochromatosis, or HH) is a hereditary disease characterized by excessive absorption of dietary iron resulting in a pathological increase in total body iron stores. Humans, like most animals, have no means to excrete excess iron. Excess iron accumulates in tissues and organs disrupting their normal function. The most susceptible organs include the liver, adrenal glands, the heart and the pancreas; patients can present with cirrhosis, adrenal insufficiency, heart failure or diabetes. The hereditary form of the disease is most common among those of Northern European ancestry, in particular those of Irish descent, and is currently the most common in the US.

Excess mucus is produced and accumulates?

Excess mucus which organelle is responsible for

What is the organelle that helps remove excess water?

contractile vacuole

What organelle gets rid of excess water?

contractile vacuole.

What is an organelle that helps remove excess water?

contractile vacuole

What is neurotransmitter that when excess or in minimal secretion produces behavior maladjustment?

What is the disease that produces excess fat?

obesity

What is cystiv 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

What is insulinoma?

It is a tumor of the pancreas that produces an excess of insulin.