Noun:

সূক্ষ্ম অংশুসমূহের বৃদ্ধি,

fibrosis's Usage Examples:

Cystic fibrosis (CF) is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, kidneys, and intestine.

Pulmonary fibrosis is a condition in which the lungs become scarred over time.

impaired liver function caused by the formation of scar tissue known as fibrosis, due to damage caused by liver disease.

Idiopathic pulmonary fibrosis (IPF) is a rare, progressive illness of the respiratory system, characterized by the thickening and stiffening of lung tissue.

Cystic fibrosis transmembrane conductance regulator (CFTR) is a membrane protein and chloride channel in vertebrates that is encoded by the CFTR gene.

Prolonged ILD may result in pulmonary fibrosis, but this is not always the case.

Idiopathic pulmonary fibrosis is interstitial lung disease for which.

Oral submucous fibrosis is a chronic, complex, premalignant (1% transformation risk) condition of the oral cavity, characterized by juxta-epithelial inflammatory.

Ivacaftor is a drug used to treat cystic fibrosis in people with certain mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

cystic fibrosis rather than the symptoms, in patients 6 years or older who have the G551D gene mutation.

In the US, 30,000 people have cystic fibrosis.

Asbestosis is a type of interstitial pulmonary fibrosis.

cystic fibrosis.

Cystic fibrosis eventually results in severe bronchiectasis in nearly all cases.

The cause in 10–50% of those without cystic fibrosis is.

a state in which steatosis is combined with inflammation and sometimes fibrosis (steatohepatitis).

Cardiac fibrosis commonly refers to the excess deposition of extracellular matrix in the cardiac muscle, but the term may also refer to an abnormal thickening.

dermatofibroma, Fibrous histiocytoma, Fibroma simplex, Nodular subepidermal fibrosis, and Sclerosing hemangioma) Histopathology of dermatofibroma, with basilar.

It occurs most often in people with asthma or cystic fibrosis.

is an oral medication used for the treatment of idiopathic pulmonary fibrosis and along with other medications for some types of non-small-cell lung.

pathologist and pediatrician who was the first person to identify cystic fibrosis and the first American physician to describe the disease.

diseases include Diabetes mellitus, Exocrine pancreatic insufficiency, Cystic fibrosis, Pseudocysts, Cysts, Congenital malformations, Neoplasms and Hemosuccus.

Synonyms:

pathology; pneumonoconiosis; pancreatic fibrosis; mucoviscidosis; fibrocystic disease of the pancreas; pneumoconiosis; CF; cystic fibrosis; myelofibrosis;

Antonyms:

good health;