cystic fibrosis

noun

Pathology.

1. a hereditary chronic disease of the exocrine glands, characterized by the production of viscid mucus that obstructs the pancreatic ducts and bronchi, leading to infection and fibrosis.

cystic fibrosis

noun

1. an inheritable disease of the exocrine glands, controlled by a recessive gene: affected children inherit defective alleles from both parents. It is characterized by chronic infection of the respiratory tract and by pancreatic insufficiency

cystic fibrosis

1. An inherited disorder of the exocrine glands, usually developing during early childhood and affecting mainly the pancreas, respiratory system, and sweat glands. It is marked by the production of abnormally thick mucus by the affected glands, usually resulting in chronic respiratory infections and impaired pancreatic function.

cystic fibrosis

1. A congenital and chronic disease that affects certain glands in the body, particularly the sweat glands, the pancreas, and the glands in the mucous membranes of the respiratory system. Cystic fibrosis causes recurring respiratory disorders (see respiration) and interferes with the production of enzymes by the pancreas.

Word History and Origins

Origin of cystic fibrosis¹

First recorded in 1950–55

Example Sentences

Some inherited diseases, including cystic fibrosis, hemophilia, and Tay Sachs disease, involve multiple genetic mutations within a person's DNA.

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We expect the company’s launch of Alyftrek in cystic fibrosis will do well over time.

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The Glaswegian was diagnosed with cystic fibrosis when just a baby, meaning she suffered breathing and digestive problems throughout her life.

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Currently, newborn babies are only given a heelprick blood test that checks for nine serious conditions, including cystic fibrosis.

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Worsening osteoporosis in older women may lead to exhaling DMS, as can the positive effects of a medication cocktail for children with cystic fibrosis.

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