fibrosis

listen to the pronunciation of fibrosis
Английский Язык - Турецкий язык
fibrosis
(isim) fibrosis
hücre aralarındaki lifli bağdokunun artması
(Tıp) Hücre aralarındaki liflerin artması, lif dejenerasyonu, fibrozit

Связанные Термины

severe fibrosis
(Tıp) ileri fibrozi
pancreatic fibrosis
pankreas fibrosis
cystic fibrosis
kistik fibrozis
cystic fibrosis
(Tıp, İlaç) Kistik fibrozis: sıklıkla çocukluk çağında başlayan, sık akciğer enfeksiyonları ve ölümle seyreden hastalık
bridging fibrosis
(Tıp) köprü fibriyosisi
fibrotic
(Tıp) Fibrozise ait, fibrotik
Английский Язык - Английский Язык
The formation of excess fibrous connective tissue in an organ
{i} excessive growth of fibrous tissue in an organ (Medicine)
The process the body uses to create scar tissue
Scar formation resulting from the repair of tissue damage If it occurs extensively in the liver, it is called cirrhosis Fibrosis does not necessarily progress to cirrhosis
Formation of scar tissue FLAMMABLE (EXPLOSIVE) LIMITS - Those concentrations of a vapor in air below or above which a flame or explosion does not occur on contact with a source of ignition See also UEL and LEL FLAMMABLE - Any substance that is easily ignited, burns intensely, or has a rapid rate of flame spread A substance with a flashpoint below 100 øF is considered flammable See COMBUSTIBLE FLASH POINT - The lowest temperature at which a liquid produces enough vapor to form an ignitable mixture with the air FR - Federal Register FUME - Finely divided particles created when volatilized solids condense in cool air, such as a heated process like welding (Fumes are technically not vapors or gases ) Fumes have particle sizes of one micrometer or less FUME FEVER - An acute condition caused by a brief high exposure to the freshly generated fumes of metals
Formation of fibrous tissue, as in a reparative or reactive process, in excess of amounts normally present
An abnormal thickening of fibrous connective tissue, usually in the lungs
replacement and disruption of the normal cellular pattern by fibrous (scar) tissue
Just means firm tissue, does not actually imply anything bad Back
Scar formation resulting from the repair of tissue damage If it occurs extensively in the liver, it is called cirrhosis Viral load: The amount of virus present in a person's blood stream It is usually measured by the PCR quantitative test and the result is given in number of virus particles per ml of blood
Formation of scar-like (fibrous) tissue top
formation of fibrous tissue as a reaction or as a repair process; may occur due to treatment and/or disease
The replacement of normal tissue with scar tissue
-A process producing scar tissue that forms as a reaction to injury or during a healing process
is the deposition of collagen, that forms a fibrose (scar) tissue, poor of blood vessels and of cells and that therefore impair liver function Liver fibrosis represents the wound healing response of the liver to a long term disease that damage it Liver fibrosis leads to cirrhosis
Scarring of tissue, making it stiffer and not as functional as normal tissue
Formation of scar tissue in response to injury
The formation of fibrous tissue, which may replace other tissue (BVD)
Refers to the presence of scar tissue or collagen fibers in any tissue In the liver, fibrosis or scarring of the liver damages the architecture and thus the functionality of the organ Fibrosis, combined with the liver's ability to regenerate, causes cirrhosis (regeneration within the scar tissue)
Scar tissue that forms in reaction to an infection or injury It can occur in the liver as a result of long-term inflammation
process by which inflamed tissue becomes scarred
development of excess fibrous connective tissue in an organ
Cross-linking between parallel strands (fibers) in a reparative or reactive process, creating an excess amount of fibers
Early scarring of the liver which may be caused by a healing response to injury, infection or inflammation
The general name for accumulation of scar tissue in the lung
Formation of fibrous tissue, as in reparative or reactive process to particulates, in excess of amounts normally present in lung tissue walls This reduces the oxygen and carbon dioxide exchange efficiency
the growth of scar tissue due to infection, inflammation, injury, or even healing

Связанные Термины

cystic fibrosis
An inherited condition in which the exocrine glands produce abnormally viscous mucus, causing chronic respiratory and digestive problems
fibrotic
Of, pertaining to, or exhibiting fibrosis

a highly fibrotic lesion.

cystic fibrosis
A hereditary disorder which affects the exocrine glands and results in the production of abnormally thick mucus, leading to the blockage of the pancreatic ducts, intestines, and bronchi
cystic fibrosis
Disease where mucus production in the lungs is abnormal, both in quantity and consistency Patients newly presenting asthma symptoms are usually tested for CF using a sweat test This is standard procedure in order to rule out CF as a cause of the patient's symptoms Cough-variant asthma and CF present very similar symptoms For more on CF, visit the Cystic Fibrosis Foundation
cystic fibrosis
A serious genetic disease of excretory glands, affecting lungs and other organs; it causes production of very thick mucus that interferes with normal digestion and breathing
cystic fibrosis
Genetic Disease with Bronchial Fluid Accumulation, resulting in Higher Susceptibility to Infections
cystic fibrosis
A recessive genetic disorder affecting the mucus lining of the lungs, leading to breathing problems and other difficulties
cystic fibrosis
An inherited disease that causes the glands to produce thick mucus
cystic fibrosis
an inherited autosomal recessive condition that causes the secretion of abnormal mucus in the lungs and problems with pancreas function and food absorption
cystic fibrosis
An inherited disease of exocrine glands, affecting most characteristically the pancreas, respiratory system, and sweat glands, usually beginning in infancy and typified by chronic respiratory infections, pancreatic insufficiency, and susceptibility to heat prostration Cirrhosis of liver occurring in childhood is common and may produce portal hypertension, splenomegaly, and hypersplenism
cystic fibrosis
A genetic disease characterized by extremely thick bodily secretions in the digestive and pulmonary systems Sticky, tenacious secretions in the lungs lead to frequent, debilitating infections, subsequent irreversible lung damage, and eventual early death due to respiratory failure Conscientious bronchial hygiene is essential in the treatment of CF
cystic fibrosis
An inherited disease that affects the pancreas, respiratory system and sweat glands, which usually begins in infancy and is characterized by chronic respiratory infection, pancreatic insufficiency and heat intolerance Prognosis is poor as there is no cure, but antibiotics have prolonged the life of manypatients
cystic fibrosis
disease of the mucus and sweat glands which causes disorders of the lungs and pancreas CF is the leading cause of chronic lung disease in children and young adults and is the most common fatal hereditary disorder affecting Caucasians in the U S
cystic fibrosis
the most common congenital disease; the child's lungs and intestines and pancreas become clogged with thick mucus; caused by defect in a single gene; there is no cure
cystic fibrosis
(sis-tik-fi-bro-sis) A disease of infants, children, adolescents, and young adults, involving the mucus secreting glands, which results in chronic pulmonary disease, pancreatic insufficiency, and abnormally high sweat electrolyte levels The affection is believed to be genetically transmitted
cystic fibrosis
An inherited disorder that causes a dysfunction of the pancreas, mucus, salivary, and sweat glands; also causes severe respiratory difficulties
cystic fibrosis
an inherited disease in which a thick mucus clogs the lungs and blocks the ducts of the pancreas
cystic fibrosis
A genetic condition characterized by thickened secretions in the lungs, bronchiectesis (see above) and repeated pulmonary infections Some patients have digestive problems, resulting in difficulty absorbing food
cystic fibrosis
A potentially lethal human disease of secretory cells, showing excess lung mucus secretion, and inherited as an autosomal recessive on chromosome 7 CF is caused by mutations in a gene encoding the cystic fibrosis membrane conductance regulator, a transmembrane protein involved in ion transport
cystic fibrosis
In the western world the most frequently determined genetic illness (autosomal recessive inherited) The gene for a chloride channel (CFTR) is affected, whose function is then limited and leads to mucilaginization, particularly in the respiratory tract Secondary infections with Pseudomonas aeruginosa frequently result from that Other organs are also affected (intestine, pancreas) The quality of life of patients is very restricted and the life expectation currently extends to the age of 30
cystic fibrosis
Cystic fibrosis is a serious disease of the glands which usually affects children and can make breathing difficult. A hereditary disease of the exocrine glands, usually developing during early childhood and affecting mainly the pancreas, respiratory system, and sweat glands. It is characterized by the production of abnormally viscous mucus by the affected glands, usually resulting in chronic respiratory infections and impaired pancreatic function. Also called mucoviscidosis. a serious medical condition, especially in children, in which breathing and digesting food is very difficult (fibrosis 1800-1900 , from fibra; FIBER). or mucoviscidosis Inherited metabolic disorder characterized by production of thick, sticky mucus. It is recessive (see recessiveness) and the most common inherited disorder (about 1 per 2,000 live births) in those of European ancestry. Concentrated mucous secretions in the lungs plug the bronchi, making breathing difficult, promoting infections, and producing chronic cough, recurrent pneumonia, and progressive loss of lung function, the usual cause of death. The secretions interfere with digestive enzymes and block nutrient absorption. Abnormally salty sweat is the basis for diagnosis of cystic fibrosis. Treatment includes enzyme supplements, a diet high in calories, protein, and fat, vigorous physical therapy, and antibiotics. Persons with cystic fibrosis once seldom survived beyond childhood; now more than half reach adulthood, though males are usually sterile
cystic fibrosis
A serious genetic disease of excretory glands, affecting lungs and other organs; it causes production of very thick mucus that interferes with normal digestion and breathing
cystic fibrosis
Disease where mucus production in the lungs is abnormal, both in quantity and consistency Patients newly presenting asthma symptoms are usually tested for CF using a sweat test This is standard procedure in order to rule out CF as a cause of the patient's symptoms Cough-variant asthma and CF present very similar symptoms For more on CF, visit the Cystic Fibrosis Foundation
cystic fibrosis
An inherited disease that affects the pancreas, respiratory system and sweat glands, which usually begins in infancy and is characterized by chronic respiratory infection, pancreatic insufficiency and heat intolerance Prognosis is poor as there is no cure, but antibiotics have prolonged the life of manypatients
cystic fibrosis
An inherited disease that causes the glands to produce thick mucus
cystic fibrosis
Genetic Disease with Bronchial Fluid Accumulation, resulting in Higher Susceptibility to Infections
cystic fibrosis
disease of the mucus and sweat glands which causes disorders of the lungs and pancreas CF is the leading cause of chronic lung disease in children and young adults and is the most common fatal hereditary disorder affecting Caucasians in the U S
cystic fibrosis
A recessive genetic disorder affecting the mucus lining of the lungs, leading to breathing problems and other difficulties
cystic fibrosis
an inherited disease in which a thick mucus clogs the lungs and blocks the ducts of the pancreas
cystic fibrosis
the most common congenital disease; the child's lungs and intestines and pancreas become clogged with thick mucus; caused by defect in a single gene; there is no cure
cystic fibrosis
A potentially lethal human disease of secretory cells, showing excess lung mucus secretion, and inherited as an autosomal recessive on chromosome 7 CF is caused by mutations in a gene encoding the cystic fibrosis membrane conductance regulator, a transmembrane protein involved in ion transport
cystic fibrosis
A genetic condition characterized by thickened secretions in the lungs, bronchiectesis (see above) and repeated pulmonary infections Some patients have digestive problems, resulting in difficulty absorbing food
cystic fibrosis
inherited children's disease in which there is fibrosis of the pancreas and respiratory infections
cystic fibrosis
An inherited disorder that causes a dysfunction of the pancreas, mucus, salivary, and sweat glands; also causes severe respiratory difficulties
cystic fibrosis
(sis-tik-fi-bro-sis) A disease of infants, children, adolescents, and young adults, involving the mucus secreting glands, which results in chronic pulmonary disease, pancreatic insufficiency, and abnormally high sweat electrolyte levels The affection is believed to be genetically transmitted
cystic fibrosis
an inherited autosomal recessive condition that causes the secretion of abnormal mucus in the lungs and problems with pancreas function and food absorption
cystic fibrosis
An inherited disease of exocrine glands, affecting most characteristically the pancreas, respiratory system, and sweat glands, usually beginning in infancy and typified by chronic respiratory infections, pancreatic insufficiency, and susceptibility to heat prostration Cirrhosis of liver occurring in childhood is common and may produce portal hypertension, splenomegaly, and hypersplenism
cystic fibrosis
In the western world the most frequently determined genetic illness (autosomal recessive inherited) The gene for a chloride channel (CFTR) is affected, whose function is then limited and leads to mucilaginization, particularly in the respiratory tract Secondary infections with Pseudomonas aeruginosa frequently result from that Other organs are also affected (intestine, pancreas) The quality of life of patients is very restricted and the life expectation currently extends to the age of 30
cystic fibrosis
A genetic disease characterized by extremely thick bodily secretions in the digestive and pulmonary systems Sticky, tenacious secretions in the lungs lead to frequent, debilitating infections, subsequent irreversible lung damage, and eventual early death due to respiratory failure Conscientious bronchial hygiene is essential in the treatment of CF
fibrotic
{s} of or pertaining to fibrosis, of or pertaining to excessive growth of fibrous tissue in an organ (Medicine)
Турецкий язык - Английский Язык
fibrosis
fibrosis

    Расстановка переносов

    fi·bro·sis

    Турецкое произношение

    faybrōsıs

    Произношение

    /fīˈbrōsəs/ /faɪˈbroʊsəs/

    Видео

    ... an “A” then you may well have cystic fibrosis.   ...
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