Cystic Fibrosis – This is an inherited pathologic condition of the secretory gland which usually affects thelungs , pancreas , liver , andintestinescausing a variety show of symptoms .
What Is Cystic Fibrosis?
Cystic Fibrosis as submit is an inherit medical condition of the secretory glands . The function of the secretory gland is to produce mucose and swither . Since this condition is inherited , it entail that it is passed from parent to the offspring through genes . It is an autosomal recessive character term which means that one defective cistron require to be inherited from both parents in guild for the young to get this condition . Cystic Fibrosis affects mainly the lungs , pancreas , liver , and intestines . This circumstance causes the mucous to become buddy-buddy and sticky . It then start up to build up in the lungs and starts blocking the air duct . This gradual buildup of mucous facilitates growth of bacterium and resultant infections which can gravely damage the lungs .
Causes Of Cystic Fibrosis
Cystic Fibrosis is an inherited disease . The main cause of Cystic Fibrosis is a blemish in the cystic fibrosis transmembrane conductance regulator gene or the CFTR factor . This gene is creditworthy for making a protein which controls campaign of table salt and piss in the trunk ’s prison cell . In individuals who are affected with Cystic Fibrosis , this gene does not work appropriately causingmucousto become thick and the sweat to become exceedingly salty .
Facts About Cystic Fibrosis
Who Is At Risk For Developing Cystic Fibrosis?
Cystic Fibrosis equally affect males and females . This status is found in people of all raceway and ethnic radical , although it is more vulgar in Caucasians and Northern Europeans . Cystic Fibrosis is also quite uncouth in people from Latin America
Symptoms Of Cystic Fibrosis
Symptoms Of Cystic Fibrosis When It Affects The Respiratory System:
Individuals affect with Cystic Fibrosis will have viscous and chummy mucous blocking the airline . This make frequent bouts of life-threatening coughing , which will be productive of thick phlegm . Sometimes , stock may also be noted in the mucous . Individuals with Cystic Fibrosis also tend to have frequentlung infectionsirresponsive to stock treatments . Cystic Fibrosis also causers frequent bouts of sinusitis . As the disease progresses , the individual may develop serious atmospheric condition likepneumothoraxor bronchiectasis .
Symptoms Of Cystic Fibrosis When It Affects The Digestive System:
In Cystic Fibrosis , the thicken mucous may immobilize tubes or duct in the pancreas thus preventing necessary enzymes from reaching the gut , which may result in foul - sense , sebaceous stools . As Cystic Fibrosis gets worse , other medical conditions may pop out propping up like
Diagnosis of Cystic Fibrosis
Treatment For Cystic Fibrosis
At present , treatment for Cystic Fibrosis is still under inquiry . Some new medications have been developed for treatment of Cystic Fibrosis but their efficacy is still under watching . The main aim for treatment of Cystic Fibrosis is :
Latest Developments In The Treatment For Cystic Fibrosis
At present , studies are being conducted on two medications namely ivacaftor with the brand name Kalydeco and lumacaftor . It is decidedly a move towards good treatment for Cystic Fibrosis , but researchers are of the opinion that more study needs to be done before assessing the full potential drop of the medications . Currently used medications taste to treat the symptom of Cystic Fibrosis , but not the root causal agency of it whereas Kalydeco targets the stem cause which is the malfunction protein that causes Cystic Fibrosis . As of now , studies mull over that only about 5 % of affected population have render positive consequence .
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