Nghĩa của từ cystic fibrosis bằng Hindi
cystic fibrosis <N.>
- श्वास~अवयव~में~संक्रमण "Research is going on in cystic fibrosis,a genetic disease"
Đặt câu có từ "cystic fibrosis"
1. Cystic Fibrosis What Is Cystic Fibrosis Cystic fibrosis (CF) is a chronic, progressive, and frequently fatal genetic (inherited) dis ease of the body’s mucus glands
2. Cystic fibrosis is a genetic disease
3. Cystic fibrosis is a recessive genetic disease
4. Add to Favorites Cystic Fibrosis Awareness Crewneck
5. Breazy Games for Cystic Fibrosis, Derby, United Kingdom
6. Cystic Fibrosis Awareness Face Mask, Cystic Fibrosis Awareness Face Mask, Purple Ribbon 100% Cotton 3 Layers Face Mask, Washable, Awareness PetJos
7. Cystic fibrosis is the Commonest fatal here-ditary disease.
8. She was clueless about how to treat cystic fibrosis.
9. Cystic fibrosis affects the sweat glands in a different way
10. Failing to reveal cystic fibrosis may be disadvantageous or even illegal.
11. Cystic fibrosis causes about half of all bronchiectasis in the United States.
12. Selective activation of cystic fibrosis transmembrane conductance regulator Cl- and HCO3- Conductances
13. Assis is an active member of the Adult Cystic Fibrosis Program at Yale
14. Cystic fibrosis is the most common fatal genetic disease in the United States.
15. Cystic fibrosis (CF) is a genetic disorder that causes problems with breathing and digestion
16. Cystic fibrosis (CF) is a genetic condition that affects a protein in the body
17. Cystic Fibrosis leverages Amply across 73 chapter organizations and raised over $319,000 in 2020
18. A mass screening has been conducted on newborns for adrenogenital syndrome, galactosemia and cystic fibrosis.
19. Cilia and the clearance of mucus are also involved in awful diseases like cystic fibrosis.
20. Cystic fibrosis is a genetic disorder that often affects multiple organ systems of the body
21. Respiratory diseases associated with finger Clubbing include chronic obstructive pulmonary disease (), lung cancer, cystic fibrosis (thick
22. Iron absorption is controlled also in cystic fibrosis chiefly by the amounts of available storage iron.
23. Bronchiectasis is sometimes called non-cystic fibrosis Bronchiectasis.This is because there is a different condition called cystic fibrosis.People who have cystic fibrosis can have lung symptoms similar to those of Bronchiectasis, but the treatments and outlook are different.
24. In children, a persistent Cough can be a sign of cystic fibrosis, a severe long-term
25. The programme of neonatal screening for cystic fibrosis, galactosemia, adrenogenital syndrome and congenital bradyacuasia has been expanded.
26. CYSTIC FIBROSIS causes Aspermia as a result of failure of development of the vas or associated structures.
27. Read in studio Scientists have made a breakthrough in the fight against the genetic disease Cystic Fibrosis.
28. Cystic fibrosis (CF) is a serious genetic condition that causes severe damage to the respiratory and digestive systems
29. Cystic fibrosis is an inherited disease characterized by an abnormality in the glands that produce sweat and mucus
30. Cystic fibrosis is characterized by abnormalities affecting certain glands (exocrine) of the body especially those that produce mucus
31. Cystic fibrosis is an inherited (genetic) condition that causes thick and sticky mucus to build up in the body
32. Discussion: In conclusion, Reye-like syndromes and dicarboxylic aciduria in infancy may be the first signs of cystic fibrosis.
33. Cystic fibrosis affects various organ systems in children and young adults, including the respiratory system, digestive system and reproductive system
34. Cystic fibrosis results when a protein that controls how salt flows in and out of cells does not work properly
35. While Cystic fibrosis is a chronic, progressive disease, improved treatments have significantly extended life expectancy for children with the condition.
36. Cystic fibrosis is a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time
37. For example, persons suffering reduced respiratory function from diseases such as cystic fibrosis seem to benefit from the increased atmospheric pressure.
38. Seeking the means to cure and control Cystic fibrosis and to improve the quality of life for those with the disease
39. In people with CF, mutations in the Cystic fibrosis transmembrane conductance regulator (CFTR) gene cause the CFTR protein to become dysfunctional.
40. TRUS usually identifies congenital bilateral absence of vas deferens; without renal agenesia, a genital form of cystic fibrosis must be evocated.
41. Risk factors include COPD, bronchiectasis, silicosis, cystic fibrosis, Aids, malignancy and achalasia, making the detection of NTM, when occurring simultaneously, more difficult.
42. Causes of secondary Clubbing include the following{ref11}: Pulmonary disease - Lung cancer,{ref12} cystic fibrosis, interstitial lung disease,{ref13} idiopathic pulmonary fibrosis,{ref14
43. People who have Cystic fibrosis have a faulty protein that affects the body’s cells, tissues, and the glands that make mucus and sweat
44. But at the age of two, Silvia was diagnosed with cystic fibrosis, an incurable disease that causes increasingly severe respiratory and digestive problems.
45. Biologics are used to prevent, treat or cure a variety of diseases including cancer, chronic kidney disease, diabetes, cystic fibrosis, and autoimmune disorders
46. Cystic fibrosis (CF) is a genetic disorder that causes mucus to build up and damage organs in the body, particularly the lungs and pancreas.
47. Cystic fibrosis, inherited metabolic disorder, the chief symptom of which is a thick, sticky mucus that clogs the respiratory tract and the gastrointestinal tract
48. 25 Pancreatic enzyme replacement therapy is given to manage pancreatic exocrine insufficiency (PEI) in cystic fibrosis (CF) and following pancreatectomy, total gastrectomy or chronic pancreatitis .
49. Aerosolized antibiotics have been tested as treatment for bacterial infections in patients with cystic fibrosis (CF), non-CF bronchiectasis (NCFB), and ventilator-associated pneumonia (VAP)
50. AirPhysio Natural Breathing Lung Expansion & Mucus Removal Device, Exerciser & Cleanse Therapy Aid Improves Sleep & Fitness, Treatment for COPD, Asthma, Bronchitis, Cystic Fibrosis,Pulmonary Relief