@@ -182,11 +182,19 @@ export function Description() {
widely, with some countries adopting more comprehensive protocols than others. Early diagnosis through
screening offers significant benefits, such as improved growth, better lung function, and overall enhanced health outcomes
<SupScrollLinklabel="40"/>{/* ehem64 */}. The discovery of the CFTR gene has further refined diagnostic techniques and underscored the crucial role of newborn screening in the early detection and management of CF. </p>
<p>Technological advancements and improved medical procedures have greatly transformed the diagnosis of Cystic Fibrosis. While newborn screening has revolutionized early detection and treatment, traditional methods such as the sweat test and symptom observation continue to play a vital role, particularly in regions where screening programs are not yet widely available.</p>
<p>Technological advancements and improved medical procedures have greatly transformed the diagnosis of Cystic Fibrosis.
While newborn screening has revolutionized early detection and treatment, traditional methods such as the sweat test and
symptom observation continue to play a vital role, particularly in regions where screening programs are not yet widely
available.</p>
</Collapsible>
<p>Another widely used method is the sweat test, which measures the concentration of chloride in a person's sweat. CF patients typically have higher-than-normal chloride levels due to defective CFTR protein function <SupScrollLinklabel="65"/><SupScrollLinklabel="66"/> . While the sweat test is non-invasive and reliable for indicating CF, it is limited in scope. For definitive diagnosis and to guide specific treatments, a genetic analysis is usually required to identify the exact CFTR mutation, such as the F508del mutation <SupScrollLinklabel="65"/><SupScrollLinklabel="66"/> .</p>
<p>Another widely used method is the sweat test, which measures the concentration of chloride in a person's sweat. CF patients
typically have higher-than-normal chloride levels due to defective CFTR protein function. While the sweat test is non-invasive and reliable for
indicating CF, it is limited in scope. For definitive diagnosis and to guide specific treatments, a genetic analysis is usually required
to identify the exact CFTR mutation, such as the F508del mutation<SupScrollLinklabel="41"/>{/* ehem66 */}.</p>
<p>Traditionally, Cystic Fibrosis (CF) has been diagnosed using the sweat test, which measures chloride levels in sweat. A chloride level below 40 mmol/L (millimoles of chloride per litre of sweat) is considered normal and unlikely to indicate CF. Levels between 40 and 60 mmol/L require further investigation, while levels above 60 mmol/L strongly suggest the presence of CF <SupScrollLinklabel="65"/> .</p>
<p>Traditionally, Cystic Fibrosis (CF) has been diagnosed using the sweat test, which measures chloride levels in sweat. A
chloride level below 40 mmol/L (millimoles of chloride per litre of sweat) is considered normal and unlikely to indicate CF.
Levels between 40 and 60 mmol/L require further investigation, while levels above 60 mmol/L strongly suggest the presence of CF<SupScrollLinklabel="41"/>{/* ehem65 */}.</p>
<p>This quick and painless test has been the gold standard for CF diagnosis for many years. Despite its accuracy, the sweat test requires specialized lab personnel and can be difficult to perform on newborns. While diagnosing CF based on symptoms can be useful, it is not always reliable, particularly in mild or atypical cases.</p>
